Stressmarq Distributor

Lab Reagents

Human IgG antibody Laboratories manufactures the stressmarq distributor reagents distributed by Genprice. The Stressmarq Distributor 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 Stressmarq Biosciences Inc.. Other Stressmarq products are available in stock. Specificity: Stressmarq Category: Distributor

Serum / Plasma information

WHI P131 (JAK3 kinase inhibitor)

SIH-485-50MG 50 mg
EUR 384
  • WHI P131 also known as Janex-1, is a reversible, potent, and specific inhibitor of JAK3. WHI P131 is cell permeable. It has been seen to inhibit glioblastoma cell adhesion and migration, as well as, thrombin-induced platelet aggregation.
Description: The substance WHI P131 is a jak3 kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white to off-white solid which is soluble in DMSO (~1 mg/ml), and DMF (~1 mg/ml).

Y 27632 (ROCK kinase inhibitor)

SIH-486-1MG 1 mg
EUR 149
  • Y 27632 is a very potent and selective ROCK1 and ROCK2 inhibitor. Y 27632 is cell permeable and is an ATP competitive inhibitor.
Description: The substance Y 27632 is a rock kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white to pale yellow powder which is soluble in DMSO (25 mg/ml), methanol (25 mg/ml), acetonitrile (<1 mg/ml), dioxan (<1 mg/ml), water (very soluble.

Y 27632 (ROCK kinase inhibitor)

SIH-486-5MG 5 mg
EUR 328
  • Y 27632 is a very potent and selective ROCK1 and ROCK2 inhibitor. Y 27632 is cell permeable and is an ATP competitive inhibitor.
Description: The substance Y 27632 is a rock kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white to pale yellow powder which is soluble in DMSO (25 mg/ml), methanol (25 mg/ml), acetonitrile (<1 mg/ml), dioxan (<1 mg/ml), water (very soluble.

ZM 306416 (VEGFR kinase inhibitor)

SIH-487-25MG 25 mg
EUR 395
  • ZM 306416 is a potent and selective VEGF receptor tyrosine kinase inhibitor. Specifically, it inhibits Flk-1 (KDR) and Flt.
Description: The substance ZM 306416 is a vegfr kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is off-white solid which is soluble in DMSO (3 mg/ml) or ethanol (1 mg/ml).

ZM 306416 (VEGFR kinase inhibitor)

SIH-487-5MG 5 mg
EUR 149
  • ZM 306416 is a potent and selective VEGF receptor tyrosine kinase inhibitor. Specifically, it inhibits Flk-1 (KDR) and Flt.
Description: The substance ZM 306416 is a vegfr kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is off-white solid which is soluble in DMSO (3 mg/ml) or ethanol (1 mg/ml).

ZM 336372 (c-Raf kinase inhibitor)

SIH-488-25MG 25 mg
EUR 574
  • ZM 336372 is a potent, specific and reversible inhibitor of the protein kinase c-Raf. It has also been shown to inhibit SAPK2/p38. ZM 336372 is cell permeable.
Description: The substance ZM 336372 is a c-raf kinase inhibitor. It is synthetically produced and has a purity of ?95%. The pure substance is white to off-white solid which is soluble in DMSO (200 mg/ml).

ZM 336372 (c-Raf kinase inhibitor)

SIH-488-5MG 5 mg
EUR 188
  • ZM 336372 is a potent, specific and reversible inhibitor of the protein kinase c-Raf. It has also been shown to inhibit SAPK2/p38. ZM 336372 is cell permeable.
Description: The substance ZM 336372 is a c-raf kinase inhibitor. It is synthetically produced and has a purity of ?95%. The pure substance is white to off-white solid which is soluble in DMSO (200 mg/ml).

ZM447439 (Aurora B kinase inhibitor)

SIH-489-10MG 10 mg
EUR 305
  • ZM447439 is a potent and selective inhibitor of Aurora B kinase. ZM447439 induces cell growth arrest mid-way through mitosis, and therefore effectively activates apoptosis.
Description: The substance ZM447439 is a aurora b kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is orange solid which is soluble in DMSO (25 mg/ml).

ZM447439 (Aurora B kinase inhibitor)

SIH-489-1MG 1 mg
EUR 137
  • ZM447439 is a potent and selective inhibitor of Aurora B kinase. ZM447439 induces cell growth arrest mid-way through mitosis, and therefore effectively activates apoptosis.
Description: The substance ZM447439 is a aurora b kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is orange solid which is soluble in DMSO (25 mg/ml).

A 769662 (AMPK kinase activator)

SIH-490-25MG 25 mg
EUR 485
  • A 769662 is a potent and reversible activator of AMP-activated protein kinase (AMPK). It has been shown to inhibit fatty acid synthesis and decreases plasma glucose and triglyceride levels in vivo.
Description: The substance A 769662 is a ampk kinase activator. It is synthetically produced and has a purity of ?99%. The pure substance is off-white solid which is soluble to 100 mM in DMSO and to 10 mM in ethanol.

A 769662 (AMPK kinase activator)

SIH-490-5MG 5 mg
EUR 171
  • A 769662 is a potent and reversible activator of AMP-activated protein kinase (AMPK). It has been shown to inhibit fatty acid synthesis and decreases plasma glucose and triglyceride levels in vivo.
Description: The substance A 769662 is a ampk kinase activator. It is synthetically produced and has a purity of ?99%. The pure substance is off-white solid which is soluble to 100 mM in DMSO and to 10 mM in ethanol.

AG 494 (EGFR kinase inhibitor)

SIH-491-10MG 10 mg
EUR 149
  • AG 494 is a potent inhibitor of epidermal growth factor receptor (EGFR) kinase. It specifically inhibits EGF receptor autophosphorylation and EGF-dependent cell growth.
Description: The substance AG 494 is a egfr kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is yellow solid which is soluble in DMSO (25 mg/ml) or 100% ethanol (25 mg/ml).

AG 494 (EGFR kinase inhibitor)

SIH-491-50MG 50 mg
EUR 401
  • AG 494 is a potent inhibitor of epidermal growth factor receptor (EGFR) kinase. It specifically inhibits EGF receptor autophosphorylation and EGF-dependent cell growth.
Description: The substance AG 494 is a egfr kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is yellow solid which is soluble in DMSO (25 mg/ml) or 100% ethanol (25 mg/ml).

AR A014418 (GSK-3 kinase inhibitor)

SIH-492-25MG 25 mg
EUR 485
  • AR A014418 is a highly selective glycogen synthase kinase 3 (GSK-3) inhibitor. GSK-3 is a serine/threonine kinase that has been implicated in pathological conditions such as diabetes and Alzheimer?s disease. AR A014418 is cell permeable.
Description: The substance AR A014418 is a gsk-3 kinase inhibitor. It is synthetically produced and has a purity of ?95%. The pure substance is white to off-white solid which is soluble in DMSO, methanol, 100% ethanol or ethyl acetate.

AR A014418 (GSK-3 kinase inhibitor)

SIH-492-5MG 5 mg
EUR 171
  • AR A014418 is a highly selective glycogen synthase kinase 3 (GSK-3) inhibitor. GSK-3 is a serine/threonine kinase that has been implicated in pathological conditions such as diabetes and Alzheimer?s disease. AR A014418 is cell permeable.
Description: The substance AR A014418 is a gsk-3 kinase inhibitor. It is synthetically produced and has a purity of ?95%. The pure substance is white to off-white solid which is soluble in DMSO, methanol, 100% ethanol or ethyl acetate.

Auranofin (IKK kinase inhibitor)

SIH-493-50MG 50 mg
EUR 149
  • Auranofin is derivative of gold and has been widely used as an anti-arthritic drug. It inhibits both leukocyte activation pathways at multiple sites and the release of inflammatory mediators from human macrophages, basophils, and pulmonary mast cells
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Description: The substance Auranofin is a ikk kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white solid which is soluble in DMSO (5 mg/ml) or 100% ethanol (4 mg/ml).

Axitinib (VEGFR kinase inhibitor)

SIH-494-10MG 10 mg
EUR 289
  • Axitinib is a potent and selective tyrosine kinase inhibitor that blocks VEGF receptors 1, 2 and 3. It has also been shown to inhibit PDGFR-? and c-Kit.
Description: The substance Axitinib is a vegfr kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is white to tan powder which is soluble to 25 mM in DMSO.