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3Mg/Ml Zymosan

Lab Reagents

Human IgG antibody Laboratories manufactures the 3mg/ml zymosan reagents distributed by Genprice. The 3Mg/Ml Zymosan reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact InVivoGen. Other 3Mg/Ml products are available in stock. Specificity: 3Mg/Ml Category: Zymosan

Chemicals information

Rat Monoclonal Anti-Mouse CD4 Pur. Low Endotoxin (Clone YTS 191.1) (rat IgG2b)

MCD004-ML 100 ug
EUR 489.6

Rat Monoclonal Anti-Mouse CD25 , Pur. Low Endotoxin (Clone PC61.5.3) (rat IgG1)

MCD025-ML 100 ug
EUR 489.6

Alpha 1 Antitrypsin Antigen

VAng-Cr3859-3mg 3 mg
EUR 967.2
Description: Alpha 1 Antitrypsin Antigen, Host/Source: Human Plasma. The purity is ≥95% by SDS-PAGE. It is shown to be non reactive for HBsAg, anti-HCV, anti-HBc, and negative for anti-HIV 1 & 2 by FDA approved tests.

ML 239

A8719-10 10 mg
EUR 268.8
Description: ML239 is the best-in-class inhibitor of the breast cancer stem cells with an IC50= 1.16 µM. [1]ML239 was a selective inhibitor an IC50= 1.18 µM against HMLE_sh_Ecad.

ML 239

A8719-25 25 mg
EUR 477.6
Description: ML239 is the best-in-class inhibitor of the breast cancer stem cells with an IC50= 1.16 µM. [1]ML239 was a selective inhibitor an IC50= 1.18 µM against HMLE_sh_Ecad.

ML 239

A8719-5 5 mg
EUR 166.8
Description: ML239 is the best-in-class inhibitor of the breast cancer stem cells with an IC50= 1.16 µM. [1]ML239 was a selective inhibitor an IC50= 1.18 µM against HMLE_sh_Ecad.

ML-354

C3058-10 10 mg
EUR 259.2
Description: IC50: 140 nMML-354 is an indole-based, proteinase-activated receptor (PAR) 4 antagonist with good potency and reasonable selectivity versus PAR1. PARs are a family of four G-protein-coupled receptors GPCRs (PAR1-PAR4) with several unique attributes, which are activated by serine proteases.

ML-354

C3058-25 25 mg
EUR 529.2
Description: IC50: 140 nMML-354 is an indole-based, proteinase-activated receptor (PAR) 4 antagonist with good potency and reasonable selectivity versus PAR1. PARs are a family of four G-protein-coupled receptors GPCRs (PAR1-PAR4) with several unique attributes, which are activated by serine proteases.

ML-354

C3058-5 5 mg
EUR 174
Description: IC50: 140 nMML-354 is an indole-based, proteinase-activated receptor (PAR) 4 antagonist with good potency and reasonable selectivity versus PAR1. PARs are a family of four G-protein-coupled receptors GPCRs (PAR1-PAR4) with several unique attributes, which are activated by serine proteases.

ML-356

C3354-1 1 mg
EUR 151.2
Description: ML-356 is an inhibitor of the thioesterase domain of fatty acid synthase with IC50 value of 334 nM.Fatty acid synthase (FAS) is a multi-enzyme protein that catalyzes fatty acid synthesis, fatty acids are related to energy production and storage, cellular structure ,hormones biosynthesis

ML-356

C3354-10 10 mg
EUR 804
Description: ML-356 is an inhibitor of the thioesterase domain of fatty acid synthase with IC50 value of 334 nM.Fatty acid synthase (FAS) is a multi-enzyme protein that catalyzes fatty acid synthesis, fatty acids are related to energy production and storage, cellular structure ,hormones biosynthesis

ML-356

C3354-5 5 mg
EUR 474
Description: ML-356 is an inhibitor of the thioesterase domain of fatty acid synthase with IC50 value of 334 nM.Fatty acid synthase (FAS) is a multi-enzyme protein that catalyzes fatty acid synthesis, fatty acids are related to energy production and storage, cellular structure ,hormones biosynthesis

ML-264

C3474-10 10 mg
EUR 289.2
Description: ML264, a potent and selective inhibitor of kruppel-like factor 5 (KLF5), inhibits the growth of colorectal cancer.

ML-264

C3474-25 25 mg
EUR 477.6
Description: ML264, a potent and selective inhibitor of kruppel-like factor 5 (KLF5), inhibits the growth of colorectal cancer.

ML-264

C3474-5 5 mg
EUR 195.6
Description: ML264, a potent and selective inhibitor of kruppel-like factor 5 (KLF5), inhibits the growth of colorectal cancer.

ML-031

C5718-10 10 mg
EUR 324
Description: ML-031 is an agonist of S1P2 with EC50 value of 1 ?M [1].

ML-031

C5718-25 25 mg
EUR 571.2
Description: ML-031 is an agonist of S1P2 with EC50 value of 1 ?M [1].

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