Theragen Bio

Research Data

Exploring MEG brain fingerprints: evaluation, pitfalls, and interpretations

Exploring MEG brain fingerprints: evaluation, pitfalls, and interpretations
Individual characterization of topics based mostly on their useful connectome (FC), termed “FC fingerprinting”, has turn out to be a extremely sought-after objective in modern neuroscience analysis. Recent useful magnetic resonance imaging (fMRI) research have demonstrated distinctive characterization and correct identification of people as an achieved process.
However, FC fingerprinting in magnetoencephalography (MEG) knowledge remains to be extensively unexplored. Here, we examine resting-state MEG knowledge from the Human Connectome Project to evaluate the MEG FC fingerprinting and its relationship with a number of components together with amplitude- and phase-coupling useful connectivity measures, spatial leakage correction, frequency bands, and behavioral significance.
To this finish, we first make use of two identification scoring strategies, differential identifiability and success price, to supply quantitative fingerprint scores for every FC measurement. Secondly, we discover the edgewise and nodal MEG fingerprinting patterns throughout the completely different frequency bands (delta, theta, alpha, beta, and gamma). Finally, we examine the cross-modality fingerprinting patterns obtained from MEG and fMRI recordings from the identical topics.
We assess the behavioral significance of FC throughout connectivity measures and imaging modalities utilizing partial least sq. correlation analyses. Our outcomes recommend that fingerprinting efficiency is closely depending on the useful connectivity measure, frequency band, identification scoring methodology, and spatial leakage correction. We report larger MEG fingerprints in phase-coupling strategies, central frequency bands (alpha and beta), and within the visible, frontoparietal, dorsal-attention, and default-mode networks.
Furthermore, cross-modality comparisons reveal a sure diploma of spatial concordance in fingerprinting patterns between the MEG and fMRI knowledge, particularly within the visible system. Finally, the multivariate correlation analyses present that MEG connectomes have robust behavioral significance, which nevertheless relies on the thought of connectivity measure and temporal scale.
This complete, albeit preliminary investigation of MEG connectome test-retest identification provides a primary characterization of MEG fingerprinting in relation to completely different methodological and electrophysiological components and contributes to the understanding of fingerprinting cross-modal relationships. We hope that this primary investigation will contribute to setting the grounds for MEG connectome identification.

Targeting platelet glycoprotein VI attenuates progressive ischemic brain harm earlier than recanalization throughout center cerebral artery occlusion in mice

In acute ischemic stroke on account of massive vessel occlusion (LVO) infarcts quickly develop into the penumbra, which represents dysfunctional, however nonetheless viable brain tissue amenable to rescue by vessel recanalization. However, infarct development and/or delayed affected person presentation are critical and frequent limitations of this to this point solely acute remedy.
Thus, a serious objective of translational analysis is to “freeze” the penumbra already throughout LVO (earlier than opening the vessel) and thereby lengthen particular person time home windows for non-futile recanalization. We used the filament occlusion mannequin of the center cerebral artery (MCAO) in mice and assessed progressive infarction underneath occlusion at 2, 3, and Four h after onset.
We present that blocking the activatory platelet receptor glycoprotein (GP)VI considerably delayed progressive neocortical infarction in comparison with isotype management antibody handled mice. Moreover, the native vascular recruitment of infiltrating neutrophils and T-cells was mitigated. In conclusion, our experimental knowledge help ongoing scientific trials blocking platelet GPVI in acute ischemic stroke.

Is transportation a threat issue for African swine fever transmission in Australia: a assessment

African swine fever (ASF) is a viral illness of the pigs that was first described in Africa throughout the early a part of the 20th century. The illness has periodically occurred outdoors of Africa, together with an ongoing epidemic in Europe and Asia that began in 2007; the illness has by no means occurred in Australia or New Zealand. Once launched into a rustic, unfold can happen by way of direct and oblique routes of transmission. Infected feral pig populations have the potential to behave as a long-term reservoir for the virus, making eradication tough. Just earlier than and all through the interval of scientific indicators, ASF virus is shed in oronasal fluids, urine, faeces and blood.
This ends in contamination of the pig’s surroundings, together with flooring, gear and autos. Transportation-related threat components subsequently are prone to play an vital position in ASF unfold, although proof to this point has been largely anecdotal. In addition to the prevailing AUSVETPLAN ASF plan, efforts must be made to enhance transportation biosecurity, from the time a pig leaves the farm to its vacation spot.
Collection of knowledge that might quantify the capabilities and capability of Australia to wash and disinfect livestock vehicles would assist to find out if non-public and/or public sector funding must be made on this space of biosecurity. No peer-reviewed analysis was recognized that described a particular course of for cleansing and disinfecting a livestock truck identified to be contaminated with ASF virus, although literature means that transportation is a vital route of transmission for transferring the virus between farms and international locations.

Global tendencies of textile waste analysis from 2005 to 2020 utilizing bibliometric evaluation

Researchers have broadly studied textile waste, however the analysis subjects improvement and efficiency tendencies on this examine space are nonetheless unclear. A bibliometric evaluation was performed to discover the worldwide scientific literature to find out cutting-edge on textile waste over the previous 16 years. Data of publications output are recognized based mostly on the Web of Science (from 2015 to 2020).
This examine used VOSviewer to analyse collaboration networks amongst authors, international locations, establishments, and writer’s key phrases in figuring out 5 predominant clusters. A complete of 3296 papers in textile waste analysis had been recognized. In this examine, a complete of 10451 authors had been concerned in textile waste analysis, and 36 authors amongst them revealed greater than ten analysis publications within the interval of this examine.
Exploring MEG brain fingerprints: evaluation, pitfalls, and interpretations
China has been in a high place in textile waste analysis transferring from Three output publications in 2005 to 91 output publications in 2020. Indian Institute of Technology System IIT System was ranked first by way of the whole publication quantity (85 publications, 2.45%). Textile wastewater and adsorption are probably the most generally used key phrases that replicate the present predominant analysis path on this discipline and obtained extra consideration in recent times.

Anti-LAMP3 antibody (Alexa-fluor 488)

STJ170004 100 µg
EUR 393
Description: The dendritic cell lysosomal-associated membrane protein (DC-LAMP)/CD208 is a type I integral transmembrane glycoprotein mostly homologous to CD68, of about 45 kDa in mouse and 90 kDa in human (glycosylation), with a bipartite C-terminal structure divided by a serine/proline rich region, a transmembrane domain and a conserved tyrosine-based lysosomal targeting motif in its cytoplasmic tail. Initially cloned as a specific marker of human mature dendritic cells (DCs), DC-LAMP has been subsequently shown to be expressed in alveolar type II pneumocytes. In both cell types, the molecule is found in the limiting membrane of intracellular multi-lamellar bodies, known as MIIC (MHC class II compartments) in human mature DCs and as lung surfactant-containing lamellar bodies in type II pneumocytes. In the latter cell type, DC-LAMP expression is also detected at the cell surface.

Anti-IL3RA antibody (Alexa-fluor 488)

STJ170009 100 µg
EUR 393
Description: IL3 exerts its biologic activity through its interaction with a cell surface receptor that consists of two subunits. The a subunit (CD123) specifically binds IL3, whereas the ß subunit is required for signaling and is common to the GMCSFR and IL5-R. 107D2.08 and 106C2.02 mAbs were obtained after mouse immunization with sorted human tonsillar PDC. Both clones strongly stain PDCs and basophils, weakly stain monocytes, CD34+ derived DCs and CD11c+ DC, while no staining is observed on T, B, NK cells as well as on mono-derived DCs. Staining with 107D2.08 and 106C2.02 mAbs are maintained on sorted PDC cultured in the presence of IL3 and CD40L, but lost when IL3 alone is added to the culture. The recognition of the IL3Ra chain by 107D2.08 and 106C2.02 was confirmed by transfection studies. 107D2.08 appeared to be the most appropriate clone for in situ studies. 107D2.08 allowed the first observation of IL3Ra+ cells in breast tumor microenvironment

Anti-CD207 antibody (Alexa-fluor 488)

STJ170014 100 µg
EUR 393
Description: Langerin/CD207 is a transmembrane C-type lectin receptor (CLR) of epidermal and mucosal Langerhans cells (LCs) that induces Birbeck's granule formation. Langerin features a single carbohydrate recognition domain (CRD) with mannose-type specificity in its extracellular portion. Langerin is unique among the CLRs in that it contains an intracellular domain with a proline-rich motif. Langerin expression has not been reported outside the DC system. (Valladeau J et al, 1999, Eur.J.Immunol., 29:2695-2704; Valladeau J et al, 2000 Immunity, 12 : 71-81; Kashihara M et al, 1986, J.Invest.Derm., 87 :602-607 Ito T et al, 1999, J.Immunol., 163 :1409-1419 ;Saeland S & Valladeau J, CD207 (Langerin) Workshop reports 2002, Leukocyte-Typing VII, White Cell Diff Antigens, D. Mason et al, Eds, Oxford University Press:306-307)

Anti-IL7R antibody (Alexa-fluor 488)

STJ170020 100 µg
EUR 393
Description: The IL7-R consists of 2 chains, IL-7R known as CD127 and common cytokine receptor chain known as CD132. A 75 to 80kDa human IL-7 receptor has been cloned that belongs to hematopoietic cytokinereceptor super family. R34-34, raised against human leukemic pre-B cells, recognized a molecule expressed on normal B cell precursors but not on mature B cells. This antibody specifically reverted IL-7 mediated growth inhibition of leukemic BCP (normal B cells precursors) and mature T cells. IL-7R expression is dramatically influenced by cytokines and antigens. This IL-7R displays both high and low affinity for its ligand (IL-7). Inhibitory and proliferative effects of IL-7 can be mediated through the same receptor on various lineages. CD4+ memory T cells express high level of IL-7R Subsets that express it generally require it, including progenitors of T and B cells, naïve and memory T cells. (Pandrau-Garcia D et al, 1994, Blood, 83, 3613-9 Mazzucchelli R et al, Nat. Review Immunol., 2007,7, 144-54)

Goat anti Mouse IgG1 (Alexa Fluor 488)

43R-1649 500 ug
EUR 570
Description: Goat anti Mouse IgG1 secondary antibody (Alexa Fluor 488)

Anti-Hu CD16 Alexa Fluor® 488

A4-646-T100 100 tests
EUR 269

AF488 Phalloidin [equivalent to Alexa Fluor® 488 phalloidin]

23153 300 Tests
EUR 306
  • R-phrase: R23, R24, R25
  • H-Phrase: H301, H311, H331
  • Symbol for dangerous compounds: T
  • UNSPEC Code: 12352200

AF488-streptavidin conjugate [Streptavidin, Alexa Fluor™ 488 Conjugate]

16891 1 mg
EUR 176
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12171501

Anti-Hu CD72 Alexa Fluor® 488

A4-310-T100 100 tests
EUR 269

Anti-Bov CD9 Alexa Fluor® 488

A4-354-C100 0.1 mg
EUR 269

Endoglin/CD105 Alexa Fluor

FC15024 100 Tests
EUR 448

Goat Anti-Mouse IgG(H+L) Alexa Fluor 488–conjugated

S0017 200ul
EUR 304

Goat Anti-Rabbit IgG(H+L) Alexa Fluor 488–conjugated

S0018 200ul
EUR 304

Donkey Anti-Rabbit IgG (H+L), Alexa Fluor® 488 Conjugated

Ab8032-001 0.5mg
EUR 435

Anti-Hu CD3 zeta (pY153) Alexa Fluor® 488

A4-686-C100 0.1 mg
EUR 269

Anti-Hu CD3 zeta (pY72) Alexa Fluor® 488

A4-712-C100 0.1 mg
EUR 269

Anti-Hu CD3 zeta (pY142) Alexa Fluor® 488

A4-730-C100 0.1 mg
EUR 269

Anti-Hu CD3 zeta (pY111) Alexa Fluor® 488

A4-737-C100 0.1 mg
EUR 269

SAM FCM (Alexa Fluor 647)

abx098902-100tests 100 tests
EUR 1233
  • Shipped within 5-10 working days.

Anti-LAMP3 (human) Monoclonal Antibody (104G4) (Alexa Fluor® 488)

M09406 100ug
EUR 565
Description: Mouse Monoclonal LAMP3 (human) Antibody (104G4) (Alexa Fluor® 488). Validated in IHC and tested in Human.

Alpha Fluor™ 488 amine

1705 1 mg
EUR 306
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12171501

Alpha Fluor™ 488 Hydroxylamine

1900 1 mg
EUR 306
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12171501

Anti-LAMP3 antibody (Alexa-fluor 546)

STJ170005 100 µg
EUR 393
Description: The dendritic cell lysosomal-associated membrane protein (DC-LAMP)/CD208 is a type I integral transmembrane glycoprotein mostly homologous to CD68, of about 45 kDa in mouse and 90 kDa in human (glycosylation), with a bipartite C-terminal structure divided by a serine/proline rich region, a transmembrane domain and a conserved tyrosine-based lysosomal targeting motif in its cytoplasmic tail. Initially cloned as a specific marker of human mature dendritic cells (DCs), DC-LAMP has been subsequently shown to be expressed in alveolar type II pneumocytes. In both cell types, the molecule is found in the limiting membrane of intracellular multi-lamellar bodies, known as MIIC (MHC class II compartments) in human mature DCs and as lung surfactant-containing lamellar bodies in type II pneumocytes. In the latter cell type, DC-LAMP expression is also detected at the cell surface.

Anti-LAMP3 antibody (Alexa-fluor 647)

STJ170006 100 µg
EUR 393
Description: The dendritic cell lysosomal-associated membrane protein (DC-LAMP)/CD208 is a type I integral transmembrane glycoprotein mostly homologous to CD68, of about 45 kDa in mouse and 90 kDa in human (glycosylation), with a bipartite C-terminal structure divided by a serine/proline rich region, a transmembrane domain and a conserved tyrosine-based lysosomal targeting motif in its cytoplasmic tail. Initially cloned as a specific marker of human mature dendritic cells (DCs), DC-LAMP has been subsequently shown to be expressed in alveolar type II pneumocytes. In both cell types, the molecule is found in the limiting membrane of intracellular multi-lamellar bodies, known as MIIC (MHC class II compartments) in human mature DCs and as lung surfactant-containing lamellar bodies in type II pneumocytes. In the latter cell type, DC-LAMP expression is also detected at the cell surface.

Anti-IL3RA antibody (Alexa-fluor 546)

STJ170010 100 µg
EUR 393
Description: IL3 exerts its biologic activity through its interaction with a cell surface receptor that consists of two subunits. The a subunit (CD123) specifically binds IL3, whereas the ß subunit is required for signaling and is common to the GMCSFR and IL5-R. 107D2.08 and 106C2.02 mAbs were obtained after mouse immunization with sorted human tonsillar PDC. Both clones strongly stain PDCs and basophils, weakly stain monocytes, CD34+ derived DCs and CD11c+ DC, while no staining is observed on T, B, NK cells as well as on mono-derived DCs. Staining with 107D2.08 and 106C2.02 mAbs are maintained on sorted PDC cultured in the presence of IL3 and CD40L, but lost when IL3 alone is added to the culture. The recognition of the IL3Ra chain by 107D2.08 and 106C2.02 was confirmed by transfection studies. 107D2.08 appeared to be the most appropriate clone for in situ studies. 107D2.08 allowed the first observation of IL3Ra+ cells in breast tumor microenvironment

Anti-IL3RA antibody (Alexa-fluor 647)

STJ170011 100 µg
EUR 393
Description: IL3 exerts its biologic activity through its interaction with a cell surface receptor that consists of two subunits. The a subunit (CD123) specifically binds IL3, whereas the ß subunit is required for signaling and is common to the GMCSFR and IL5-R. 107D2.08 and 106C2.02 mAbs were obtained after mouse immunization with sorted human tonsillar PDC. Both clones strongly stain PDCs and basophils, weakly stain monocytes, CD34+ derived DCs and CD11c+ DC, while no staining is observed on T, B, NK cells as well as on mono-derived DCs. Staining with 107D2.08 and 106C2.02 mAbs are maintained on sorted PDC cultured in the presence of IL3 and CD40L, but lost when IL3 alone is added to the culture. The recognition of the IL3Ra chain by 107D2.08 and 106C2.02 was confirmed by transfection studies. 107D2.08 appeared to be the most appropriate clone for in situ studies. 107D2.08 allowed the first observation of IL3Ra+ cells in breast tumor microenvironment

Anti-CD207 antibody (Alexa-fluor 546)

STJ170015 100 µg
EUR 393
Description: Langerin/CD207 is a transmembrane C-type lectin receptor (CLR) of epidermal and mucosal Langerhans cells (LCs) that induces Birbeck's granule formation. Langerin features a single carbohydrate recognition domain (CRD) with mannose-type specificity in its extracellular portion. Langerin is unique among the CLRs in that it contains an intracellular domain with a proline-rich motif. Langerin expression has not been reported outside the DC system. (Valladeau J et al, 1999, Eur.J.Immunol., 29:2695-2704; Valladeau J et al, 2000 Immunity, 12 : 71-81; Kashihara M et al, 1986, J.Invest.Derm., 87 :602-607 Ito T et al, 1999, J.Immunol., 163 :1409-1419 ;Saeland S & Valladeau J, CD207 (Langerin) Workshop reports 2002, Leukocyte-Typing VII, White Cell Diff Antigens, D. Mason et al, Eds, Oxford University Press:306-307)

Anti-CD207 antibody (Alexa-fluor 647)

STJ170016 100 µg
EUR 393
Description: Langerin/CD207 is a transmembrane C-type lectin receptor (CLR) of epidermal and mucosal Langerhans cells (LCs) that induces Birbeck's granule formation. Langerin features a single carbohydrate recognition domain (CRD) with mannose-type specificity in its extracellular portion. Langerin is unique among the CLRs in that it contains an intracellular domain with a proline-rich motif. Langerin expression has not been reported outside the DC system. (Valladeau J et al, 1999, Eur.J.Immunol., 29:2695-2704; Valladeau J et al, 2000 Immunity, 12 : 71-81; Kashihara M et al, 1986, J.Invest.Derm., 87 :602-607 Ito T et al, 1999, J.Immunol., 163 :1409-1419 ;Saeland S & Valladeau J, CD207 (Langerin) Workshop reports 2002, Leukocyte-Typing VII, White Cell Diff Antigens, D. Mason et al, Eds, Oxford University Press:306-307)

Anti-IL7R antibody (Alexa-fluor 546)

STJ170021 100 µg
EUR 393
Description: The IL7-R consists of 2 chains, IL-7R known as CD127 and common cytokine receptor chain known as CD132. A 75 to 80kDa human IL-7 receptor has been cloned that belongs to hematopoietic cytokinereceptor super family. R34-34, raised against human leukemic pre-B cells, recognized a molecule expressed on normal B cell precursors but not on mature B cells. This antibody specifically reverted IL-7 mediated growth inhibition of leukemic BCP (normal B cells precursors) and mature T cells. IL-7R expression is dramatically influenced by cytokines and antigens. This IL-7R displays both high and low affinity for its ligand (IL-7). Inhibitory and proliferative effects of IL-7 can be mediated through the same receptor on various lineages. CD4+ memory T cells express high level of IL-7R Subsets that express it generally require it, including progenitors of T and B cells, naïve and memory T cells. (Pandrau-Garcia D et al, 1994, Blood, 83, 3613-9 Mazzucchelli R et al, Nat. Review Immunol., 2007,7, 144-54)

Anti-IL7R antibody (Alexa-fluor 647)

STJ170022 100 µg
EUR 393
Description: The IL7-R consists of 2 chains, IL-7R known as CD127 and common cytokine receptor chain known as CD132. A 75 to 80kDa human IL-7 receptor has been cloned that belongs to hematopoietic cytokinereceptor super family. R34-34, raised against human leukemic pre-B cells, recognized a molecule expressed on normal B cell precursors but not on mature B cells. This antibody specifically reverted IL-7 mediated growth inhibition of leukemic BCP (normal B cells precursors) and mature T cells. IL-7R expression is dramatically influenced by cytokines and antigens. This IL-7R displays both high and low affinity for its ligand (IL-7). Inhibitory and proliferative effects of IL-7 can be mediated through the same receptor on various lineages. CD4+ memory T cells express high level of IL-7R Subsets that express it generally require it, including progenitors of T and B cells, naïve and memory T cells. (Pandrau-Garcia D et al, 1994, Blood, 83, 3613-9 Mazzucchelli R et al, Nat. Review Immunol., 2007,7, 144-54)

Anti-Langerin (human) Monoclonal Antibody (DCGM4/122D5) (Alexa Fluor® 488)

M02316 100ug
EUR 580
Description: Mouse Monoclonal Langerin (human) Antibody (DCGM4/122D5) (Alexa Fluor® 488). Validated in IHC and tested in Human.

Alpha Fluor™ 488 NHS Ester

1812 1 mg
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12171501

Streptavidin-Alexa488 (Alexas fluor 488) conjugate

SV-A488-100 100 tests
EUR 225

Rabbit Anti-Rat IgG (H+L)-Alexa 488 Fluor conjugate (adsorbed with human IgG)

50336 0.5 ml
EUR 225

Alpha Fluor™ 532 acid [equivalent to Alexa Fluor™ 532 acid]

1795 10 mg
EUR 393
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12171501

Mouse IgG1-Alexa 488 conjugate (isotype control)

20102-101-A488 50 Tests
EUR 263

AF350 Phalloidin [equivalent to Alexa Fluor® 350 phalloidin]

23150 300 Tests
EUR 306
  • R-phrase: R23, R24, R25
  • H-Phrase: H301, H311, H331
  • Symbol for dangerous compounds: T
  • UNSPEC Code: 12352200

AF594 Phalloidin [equivalent to Alexa Fluor® 594 phalloidin]

23158 300 Tests
EUR 306
  • R-phrase: R23, R24, R25
  • H-Phrase: H301, H311, H331
  • Symbol for dangerous compounds: T
  • UNSPEC Code: 12352200

AF350-streptavidin conjugate [Streptavidin, Alexa Fluor™ 350 Conjugate]

16890 1 mg
EUR 176
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12171501

AF594-streptavidin conjugate [Streptavidin, Alexa Fluor™ 594 Conjugate]

16892 1 mg
EUR 176
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12171501

Donkey anti Goat IgG (H + L) (Alexa Fluor 594)

43R-ID005AF 500 ug
EUR 338
Description: Donkey anti Goat IgG (H + L) secondary antibody (Alexa Fluor 594)

Donkey anti Rat IgG (H + L) (Alexa Fluor 594)

43R-ID022AF 500 ug
EUR 364
Description: Donkey anti Rat IgG (H + L) secondary antibody (Alexa Fluor 594)

Donkey anti Goat IgG (H + L) (Alexa Fluor 647)

43R-ID028AF 500 ug
EUR 430
Description: Donkey anti Goat IgG (H + L) secondary antibody (Alexa Fluor 647)

Donkey anti Rat IgG (H + L) (Alexa Fluor 594)

43R-ID047AF 500 ug
EUR 462
Description: Donkey anti Rat IgG (H + L) secondary antibody (Alexa Fluor 594)

Donkey anti Chicken IgY (H + L) (Alexa Fluor 594)

43R-ID056AF 500 ug
EUR 343
Description: Donkey anti Chicken IgY secondary antibody (H + L) (Alexa Fluor 594)

Donkey anti Chicken IgY (H + L) (Alexa Fluor 647)

43R-ID060AF 300 ug
EUR 425
Description: Donkey anti Chicken IgY (H + L) (Fab'2) (Alexa Fluor 647)

Rabbit anti Chicken IgY (H + L) (Alexa Fluor 594)

43R-IR016AF 1 mg
EUR 281
Description: Rabbit anti Chicken IgY (H + L) secondary antibody (Alexa Fluor 594)

Anti-Hu CD30 Alexa Fluor® 700

A7-455-T100 100 tests
EUR 269

Anti-Hu CD94 Alexa Fluor® 700

A7-727-T100 100 tests
EUR 269

Anti-Hu CD56 Alexa Fluor® 700

A7-789-T100 100 tests
EUR 269

Goat Anti-Mouse IgG(H+L) Alexa Fluor 594–conjugated

S0005 200ul
EUR 376

Goat Anti-Rabbit IgG(H+L) Alexa Fluor 594–conjugated

S0006 200ul
EUR 376

Goat Anti-Rabbit IgG(H+L) Alexa Fluor 647–conjugated

S0013 200ul
EUR 304

Goat Anti-Mouse IgG(H+L) Alexa Fluor 647–conjugated

S0014 200ul
EUR 304

Mouse pre-microRNA Expression Construct mir-488

MMIR-488-PA-1 Bacterial Streak
EUR 684
  • Category: MicroRNA Tools

Donkey anti Goat IgG (H + L) (Fab 2) (Alexa Fluor 594)

43R-ID012AF 300 ug
EUR 410
Description: Donkey anti Goat IgG (H + L) secondary antibody (Fab'2) (Alexa Fluor 594)

Donkey Anti-Goat IgG (H+L), Alexa Fluor® 594 Conjugated

Ab8011-001 1mg
EUR 334

Anti-Hu CD3 zeta (pY153) Alexa Fluor® 647

A6-686-C100 0.1 mg
EUR 269

Anti-Hu CD3 zeta (pY72) Alexa Fluor® 647

A6-712-C100 0.1 mg
EUR 269

Anti-Hu CD3 zeta (pY142) Alexa Fluor® 647

A6-730-C100 0.1 mg
EUR 269

Anti-Hu CD3 zeta (pY111) Alexa Fluor® 647

A6-737-C100 0.1 mg
EUR 269

Rabbit Anti-Rat IgG (H+L)-Alexa 594 Fluor conjugate (adsorbed with human IgG)

50337 0.5 ml
EUR 225

Recombinant (E.Coli) Hepatitis C Virus (HCV) NS5 Genotype-2a 

RP-488 100 ug
EUR 286

Tide Fluor 2-LL-37

H-8286.0100 0.1mg
EUR 312
Description: Sum Formula: C205H340N60O53+dye

Tide Fluor 2-LL-37

H-8286.0500 0.5mg
EUR 1017
Description: Sum Formula: C205H340N60O53+dye

Anti-Cytokeratins Alexa Fluor488

A4-108-C025 0.025 mg
EUR 175

Anti-Cytokeratins Alexa Fluor488

A4-108-C100 0.1 mg
EUR 310

Anti-PSMA Alexa Fluor488

A4-539-C025 0.025 mg
EUR 227

Anti-PSMA Alexa Fluor488

A4-539-C100 0.1 mg
EUR 414

Anti-FoxP3 Alexa Fluor488

A4-601-C025 0.025 mg
EUR 201

Anti-FoxP3 Alexa Fluor488

A4-601-C100 0.1 mg
EUR 362

Anti-Phosphotyrosine Alexa Fluor647

A6-263-C025 0.025 mg
EUR 154

Anti-Phosphotyrosine Alexa Fluor647

A6-263-C100 0.1 mg
EUR 269

Anti-LCK Alexa Fluor647

A6-269-C025 0.025 mg
EUR 206

Anti-LCK Alexa Fluor647

A6-269-C100 0.1 mg
EUR 373

Anti-FoxP3 Alexa Fluor647

A6-601-C025 0.025 mg
EUR 201

Anti-FoxP3 Alexa Fluor647

A6-601-C100 0.1 mg
EUR 362

Monoclonal Anti-Monkey IgG-Alexa 488 Conj. (specific for monkey; no reactivity with human or animals IgG)

70030-AF488 50 tests
EUR 347

CellBriteâ„¢ Fix 488

30090 1KIT
EUR 644
Description: Minimum order quantity: 1 unit of 1KIT

Metal Fluor™ Zn-520, AM

21263 1 mg
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

Alpha Fluor™ 532 NHS Ester

1819 1 mg
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12171501

Alpha Fluor™ 594 C5 Maleimide

1891 1 mg
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12171501

Helix Fluor™ 6-JOE Phosphoramidite

6046 100 umoles
EUR 50
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12171501

Tide Fluor 2-LL-37 (scrambled)

H-8288.0100 0.1mg
EUR 312
Description: Sum Formula: C205H340N60O53+dye

Tide Fluor 2-LL-37 (scrambled)

H-8288.0500 0.5mg
EUR 1017
Description: Sum Formula: C205H340N60O53+dye

Tide Fluor 5WS-o-Conotoxin GVIA

H-8356.0100 0.1mg
EUR 1146
Description: Sum Formula: C120H182N38O43S6+dye

Streptavidin-Alexa594 (Alexas fluor 594) conjugate

SV-A594-100 100 tests
EUR 225

Anti-Cytokeratin 18 Alexa Fluor488

A4-106-C025 0.025 mg
EUR 186

Anti-Cytokeratin 18 Alexa Fluor488

A4-106-C100 0.1 mg
EUR 331

Anti-Cytokeratin 19 Alexa Fluor488

A4-120-C025 0.025 mg
EUR 186

Anti-Cytokeratin 19 Alexa Fluor488

A4-120-C100 0.1 mg
EUR 331

Anti-Ki-67 Alexa Fluor488

A4-155-T025 25 tests
EUR 154

Anti-Ki-67 Alexa Fluor488

A4-155-T100 100 tests
EUR 269

Anti-Hu CD45 Alexa Fluor488

A4-160-T100 100 tests
EUR 269

Anti-Hu CD193 Alexa Fluor488

A4-161-T100 100 tests
EUR 269

Anti-Hu CD279 Alexa Fluor488

A4-176-T100 100 tests
EUR 269

Anti-Hu CD43 Alexa Fluor488

A4-220-T025 25 tests
EUR 154

Anti-Hu CD43 Alexa Fluor488

A4-220-T100 100 tests
EUR 269

Anti-Hu CD44 Alexa Fluor488

A4-221-T025 25 tests
EUR 154

Anti-Hu CD44 Alexa Fluor488

A4-221-T100 100 tests
EUR 269

Anti-Hu CD45 Alexa Fluor488

A4-222-T025 25 tests
EUR 154

Anti-Hu CD45 Alexa Fluor488

A4-222-T100 100 tests
EUR 269

Anti-Hu CD55 Alexa Fluor488

A4-230-T025 25 tests
EUR 154

Anti-Hu CD55 Alexa Fluor488

A4-230-T100 100 tests
EUR 269

Anti-Hu CD50 Alexa Fluor488

A4-266-T025 25 tests
EUR 154

Anti-Hu CD50 Alexa Fluor488

A4-266-T100 100 tests
EUR 269

Anti-Hu CD31 Alexa Fluor488

A4-273-T025 25 tests
EUR 154

Anti-Hu CD31 Alexa Fluor488

A4-273-T100 100 tests
EUR 269

Anti-Hu CD147 Alexa Fluor488

A4-274-T025 25 tests
EUR 154

Anti-Hu CD147 Alexa Fluor488

A4-274-T100 100 tests
EUR 269

Anti-Hu CD34 Alexa Fluor488

A4-297-T025 25 tests
EUR 154

Anti-Hu CD34 Alexa Fluor488

A4-297-T100 100 tests
EUR 269

Anti-Hu CD105 Alexa Fluor488

A4-298-T025 25 tests
EUR 154

Anti-Hu CD105 Alexa Fluor488

A4-298-T100 100 tests
EUR 269

Anti-Hu CD41 Alexa Fluor488

A4-309-T025 25 tests
EUR 154

Anti-Hu CD41 Alexa Fluor488

A4-309-T100 100 tests
EUR 269

Anti-Hu CD72 Alexa Fluor488

A4-310-T025 25 tests
EUR 154

Anti-Hu CD63 Alexa Fluor488

A4-343-T025 25 tests
EUR 154

Anti-Hu CD63 Alexa Fluor488

A4-343-T100 100 tests
EUR 269

Anti-Hu CD13 Alexa Fluor488

A4-396-T025 25 tests
EUR 154

Anti-Hu CD13 Alexa Fluor488

A4-396-T100 100 tests
EUR 269

Anti-HLA-G Alexa Fluor488

A4-431-C025 0.025 mg
EUR 217

Anti-HLA-G Alexa Fluor488

A4-431-C100 0.1 mg
EUR 394

Anti-HLA-G Alexa Fluor488

A4-437-C025 0.025 mg
EUR 217

Anti-HLA-G Alexa Fluor488

A4-437-C100 0.1 mg
EUR 394

Anti-Hu CD300a Alexa Fluor488

A4-501-T100 100 tests
EUR 269

Anti-HLA-A2 Alexa Fluor488

A4-556-T025 25 tests
EUR 154

Anti-HLA-A2 Alexa Fluor488

A4-556-T100 100 tests
EUR 269

Anti-CD3 zeta Alexa Fluor488

A4-568-C100 0.1 mg
EUR 269

Anti-Ms CD8a Alexa Fluor488

A4-579-C025 0.025 mg
EUR 139

Anti-Ms CD8a Alexa Fluor488

A4-579-C100 0.1 mg
EUR 238

Anti-Hu CD326 Alexa Fluor488

A4-582-T100 100 tests
EUR 269

Anti-Hu CD3 Alexa Fluor488

A4-631-T100 100 tests
EUR 269

Anti-Hu CD16 Alexa Fluor488

A4-646-T025 25 tests
EUR 154

Anti-Hu CD150 Alexa Fluor488

A4-660-T100 100 tests
EUR 269

Anti-Hu CD107a Alexa Fluor488

A4-671-T025 25 tests
EUR 154

Anti-Hu CD107a Alexa Fluor488

A4-671-T100 100 tests
EUR 269

Anti-Hu CD107b Alexa Fluor488

A4-672-T025 25 tests
EUR 154

Anti-Hu CD107b Alexa Fluor488

A4-672-T100 100 tests
EUR 269

Anti-Hu CD73 Alexa Fluor488

A4-675-T100 100 tests
EUR 269

Anti-Hu CD11b Alexa Fluor488

A4-681-T025 25 tests
EUR 154

Anti-Hu CD11b Alexa Fluor488

A4-681-T100 100 tests
EUR 269

Anti-Hu CD35 Alexa Fluor488

A4-703-T100 100 tests
EUR 269

Anti-Hu CD305 Alexa Fluor488

A4-713-T100 100 tests
EUR 269

Anti-Hu CD161 Alexa Fluor488

A4-729-T100 100 tests
EUR 269

Anti-Hu CD144 Alexa Fluor488

A4-770-T100 100 tests
EUR 269

Anti-HLA-ABCE Alexa Fluor488

A4-813-C100 0.1 mg
EUR 373

Anti-Ki-67 Alexa Fluor647

A6-155-T025 25 tests
EUR 154

Anti-Ki-67 Alexa Fluor647

A6-155-T100 100 tests
EUR 269

Anti-Hu CD45 Alexa Fluor647

A6-160-T100 100 tests
EUR 269

Anti-Hu CD193 Alexa Fluor647

A6-161-T100 100 tests
EUR 269

Anti-Hu CD279 Alexa Fluor647

A6-176-T100 100 tests
EUR 269

Anti-Hu CD273 Alexa Fluor647

A6-178-T100 100 tests
EUR 269

Anti-Hu CD231 Alexa Fluor647

A6-200-T100 100 tests
EUR 269

Anti-Hu CD9 Alexa Fluor647

A6-208-T025 25 tests
EUR 154

Anti-Hu CD9 Alexa Fluor647

A6-208-T100 100 tests
EUR 269

Anti-Hu CD45 Alexa Fluor647

A6-222-T025 25 tests
EUR 154

Anti-Hu CD45 Alexa Fluor647

A6-222-T100 100 tests
EUR 269

Anti-Hu CD45RB Alexa Fluor647

A6-224-T025 25 tests
EUR 154

Anti-Hu CD45RB Alexa Fluor647

A6-224-T100 100 tests
EUR 269

Anti-Hu CD55 Alexa Fluor647

A6-230-T025 25 tests
EUR 154

Anti-Hu CD55 Alexa Fluor647

A6-230-T100 100 tests
EUR 269

Anti-Hu CD59 Alexa Fluor647

A6-233-T025 25 tests
EUR 154

Anti-Hu CD59 Alexa Fluor647

A6-233-T100 100 tests
EUR 269

Anti-Hu CD71 Alexa Fluor647

A6-235-T025 25 tests
EUR 154

Anti-Hu CD71 Alexa Fluor647

A6-235-T100 100 tests
EUR 269

Anti-Hu CD21 Alexa Fluor647

A6-306-T025 25 tests
EUR 154

Anti-Hu CD21 Alexa Fluor647

A6-306-T100 100 tests
EUR 269

Anti-Hu CD177 Alexa Fluor647

A6-314-T025 25 tests
EUR 154

Anti-Hu CD177 Alexa Fluor647

A6-314-T100 100 tests
EUR 269

Anti-Hu CD222 Alexa Fluor647

A6-315-T025 25 tests
EUR 154

Anti-Hu CD222 Alexa Fluor647

A6-315-T100 100 tests
EUR 269

Anti-Hu CD30 Alexa Fluor647

A6-455-T025 25 tests
EUR 154

Anti-Hu CD30 Alexa Fluor647

A6-455-T100 100 tests
EUR 269

Anti-gamma-Tubulin Alexa Fluor647

A6-465-C025 0.025 mg
EUR 217

Anti-gamma-Tubulin Alexa Fluor647

A6-465-C100 0.1 mg
EUR 394

Anti-Hu CD264 Alexa Fluor647

A6-519-C100 0.1 mg
EUR 269

Anti-Hu CD69 Alexa Fluor647

A6-552-T025 25 tests
EUR 154

Anti-Hu CD69 Alexa Fluor647

A6-552-T100 100 tests
EUR 269

Anti-HLA-A2 Alexa Fluor647

A6-556-T025 25 tests
EUR 154

Anti-HLA-A2 Alexa Fluor647

A6-556-T100 100 tests
EUR 269

Anti-Hu CD326 Alexa Fluor647

A6-581-T025 25 tests
EUR 154

Anti-Hu CD326 Alexa Fluor647

A6-581-T100 100 tests
EUR 269

Anti-Hu CD326 Alexa Fluor647

A6-582-T100 100 tests
EUR 269

Anti-Hu CD158d Alexa Fluor647

A6-609-T100 100 tests
EUR 269

Anti-Hu CD3 Alexa Fluor647

A6-631-T100 100 tests
EUR 269

Anti-Hu CD209 Alexa Fluor647

A6-640-T100 100 tests
EUR 269

Anti-Hu CD64 Alexa Fluor647

A6-644-T025 25 tests
EUR 154

Anti-Hu CD64 Alexa Fluor647

A6-644-T100 100 tests
EUR 269

Anti-Hu CD16 Alexa Fluor647

A6-646-T025 25 tests
EUR 154

Anti-Hu CD16 Alexa Fluor647

A6-646-T100 100 tests
EUR 269

Anti-Hu CD150 Alexa Fluor647

A6-660-T100 100 tests
EUR 269

Anti-Hu CD73 Alexa Fluor647

A6-675-T100 100 tests
EUR 269

Anti-HLA-DR Alexa Fluor647

A6-690-T025 25 tests
EUR 154

Anti-HLA-DR Alexa Fluor647

A6-690-T100 100 tests
EUR 269

Anti-Hu CD161 Alexa Fluor647

A6-729-T100 100 tests
EUR 269

Anti-Hu CD200 Alexa Fluor647

A6-746-T100 100 tests
EUR 269

Anti-Hu CD160 Alexa Fluor647

A6-750-T100 100 tests
EUR 269

Anti-Hu CD243 Alexa Fluor647

A6-764-T100 100 tests
EUR 269
Based on key phrase cluster evaluation outputs, textile waste analysis may be categorized into 5 forms of clusters, particularly (1) pollutant compositions, (2) part of textile wastewater, (3) therapy strategies for textile wastewater, (4) impact mechanism of textile wastewater, and (5) recyclability of textile waste.

Leave a Reply

Your email address will not be published. Required fields are marked *