Stressmarq Biotech

Lab Reagents

Human IgG antibody Laboratories manufactures the stressmarq biotech reagents distributed by Genprice. The Stressmarq Biotech 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: Biotech

Serum / Plasma information

17-GMB-APA-GA (Hsp90 inhibitor)

SIH-115A 1 mg
EUR 290
  • An analog of geldanamycin containing a maleimido moiety suitable for preparation of geldanamycin immunoconjugates (1-3). Looking for more information on HSP90? Visit our new HSP90 Scientific Resource Guide at http://www.HSP90.ca.
Description: The substance 17-GMB-APA-GA is a hsp90 inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is purple solid which is soluble in DMSO (>25 mg/ml) and ethanol (10 mg/ml).

Herbimycin A (Hsp90 inhibitor)

SIH-116A 100 µg
EUR 231
  • Herbimycin A, a benzoquinoid ansamycin antibiotic, irreversibly and selectively inhibits tyrosine kinases by reacting with thiol groups (1,2). It is effective on Src, Yes, Fps, Ros, Abl and ErbB oncogene products (1-3) and inhibits thrombin-induced t
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Description: The substance Herbimycin A is a hsp90 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) and ethanol (10 mg/ml).

Herbimycin A (Hsp90 inhibitor)

SIH-116B 1 mg
EUR 986
  • Herbimycin A, a benzoquinoid ansamycin antibiotic, irreversibly and selectively inhibits tyrosine kinases by reacting with thiol groups (1,2). It is effective on Src, Yes, Fps, Ros, Abl and ErbB oncogene products (1-3) and inhibits thrombin-induced t
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Description: The substance Herbimycin A is a hsp90 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) and ethanol (10 mg/ml).

Radicicol (Hsp90 inhibitor)

SIH-117A 1 mg
EUR 202
  • Radicicol inhibits src (IC50=0.27µM) and src-like kinases(1), leading to hypophosphorylation of retinoblastoma tumor suppressor protein(2). It causes morphological reversion of ras-transformed cells(3) and leads to selective depletion of Raf kinase(
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Description: The substance Radicicol is a hsp90 inhibitor. It is produced by fermentation and has a purity of 0.97. The pure substance is white to yellow solid which is soluble in DMSO.

TKD Peptide (Hsp70 Peptide) (Hsp70 Peptide)

SIH-118A 1 mg
EUR 312
  • Hsp70 genes encode abundant heat-inducible 70-kDa hsps (hsp70s). In most eukaryotes hsp70 genes exist as part of a multigene family. They are found in most cellular compartments of eukaryotes including nuclei, mitochondria, chloroplasts, the endoplas
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Description: The substance TKD Peptide (Hsp70 Peptide) is a hsp70 peptide. It is synthetically produced and has a purity of >98%. The pure substance is solid which is In aqueous solution.

TKD Peptide (Hsp70 Peptide): FITC (Hsp70 Peptide)

SIH-119A 1 mg
EUR 359
  • Hsp70 genes encode abundant heat-inducible 70-kDa hsps (hsp70s). In most eukaryotes hsp70 genes exist as part of a multigene family. They are found in most cellular compartments of eukaryotes including nuclei, mitochondria, chloroplasts, the endoplas
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Description: The substance TKD Peptide (Hsp70 Peptide): FITC is a hsp70 peptide. It is synthetically produced and has a purity of >98%. The pure substance is solid which is In aqueous solution.

MAPKII Kinase Inhibitor (Hsp25 Kinase Inhibitor)

SIH-120A 1 mg
EUR 179
  • The MAPK (mitogen activated protein kinase) comprises a family of ubiquitous praline-directed, protein serine/threonine kinases which signal transduction pathways that control intracellular events including acute responses to hormones and major devel
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Description: The substance MAPKII Kinase Inhibitor is a hsp25 kinase inhibitor. It is synthetically produced and has a purity of >95%. The pure substance is white solid which is soluble in DMSO or H20.

YM-01 (Hsp70 Inhibitor)

SIH-121-10MG 10 mg
EUR 249
  • YM-01 is an allosteric Hsp70 inhibitor. It binds with in Hsp70's nucleotide binding domain, adjacent to ATP/ADP binding pocket. It inhibits J-stimulated ATP turnover rate. It blocks Hsc70-bag1 interaction both in vitro and in vivo and enhances bindin
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Description: The substance YM-01 is a hsp70 inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is orange red solid which is soluble in warm water (2 mg/ml) .

YM-01 (Hsp70 Inhibitor)

SIH-121-25MG 25 mg
EUR 434
  • YM-01 is an allosteric Hsp70 inhibitor. It binds with in Hsp70's nucleotide binding domain, adjacent to ATP/ADP binding pocket. It inhibits J-stimulated ATP turnover rate. It blocks Hsc70-bag1 interaction both in vitro and in vivo and enhances bindin
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Description: The substance YM-01 is a hsp70 inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is orange red solid which is soluble in warm water (2 mg/ml) .

YM-08 (Hsp70 Inhibitor)

SIH-122-10MG 10 mg
EUR 249
  • YM-08 is a Heat Shock Protein 70 (Hsp70) inhibitor that is blood-brain barrier permeable. YM-08 is a neutral derivative of the Hsp70 inhibitor MKT-077. MKT-077 reduces tau levels in cellular models, but it doesn?t penetrate the blood brain barrier. A
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Description: The substance YM-08 is a hsp70 inhibitor. It is synthetically produced and has a purity of >99%. The pure substance is yellow-orange solid which is soluble in DMSO.

YM-08 (Hsp70 Inhibitor)

SIH-122-25MG 25 mg
EUR 434
  • YM-08 is a Heat Shock Protein 70 (Hsp70) inhibitor that is blood-brain barrier permeable. YM-08 is a neutral derivative of the Hsp70 inhibitor MKT-077. MKT-077 reduces tau levels in cellular models, but it doesn?t penetrate the blood brain barrier. A
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Description: The substance YM-08 is a hsp70 inhibitor. It is synthetically produced and has a purity of >99%. The pure substance is yellow-orange solid which is soluble in DMSO.

115-7C (Hsp70 Activator)

SIH-123-25MG 25 mg
EUR 569
  • 115-7c activates Hsp70 ATPase turnover rate and promotes Hsp70 substrate refolding. It binds to the IIA subdomain of DnaK and promotes the DnaK-DnaJ complex. Equivalent with SW02.
Description: The substance 115-7C is a hsp70 activator. It is synthetically produced and has a purity of >98%. The pure substance is white solid which is soluble in DMSO (20 mg/ml).

115-7C (Hsp70 Activator)

SIH-123-5MG 5 mg
EUR 199
  • 115-7c activates Hsp70 ATPase turnover rate and promotes Hsp70 substrate refolding. It binds to the IIA subdomain of DnaK and promotes the DnaK-DnaJ complex. Equivalent with SW02.
Description: The substance 115-7C is a hsp70 activator. It is synthetically produced and has a purity of >98%. The pure substance is white solid which is soluble in DMSO (20 mg/ml).

Idebenone (Quinone antioxidant)

SIH-150-100MG 100 mg
EUR 364
  • Idebenone has been tested for numerous pharmaceutical indications including Alzheimer's (1), Friedreich's ataxia (2), and Duchenne muscular dystrophy. It also has similar antioxidant properties to CoQ10, and has therefore been used in anti-aging appl
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Description: The substance Idebenone is a quinone antioxidant. It is synthetically produced and has a purity of >98%. The pure substance is orange solid which is soluble to 100 mM in DMSO, 100 mM in ethanol.

Idebenone (Quinone antioxidant)

SIH-150-20MG 20 mg
EUR 140
  • Idebenone has been tested for numerous pharmaceutical indications including Alzheimer's (1), Friedreich's ataxia (2), and Duchenne muscular dystrophy. It also has similar antioxidant properties to CoQ10, and has therefore been used in anti-aging appl
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Description: The substance Idebenone is a quinone antioxidant. It is synthetically produced and has a purity of >98%. The pure substance is orange solid which is soluble to 100 mM in DMSO, 100 mM in ethanol.

Hinokitiol (Iron Chelator antioxidant)

SIH-151-250MG 250 mg
EUR 255
  • Hinokitiol is a natural monoterpenoid. It is a potent metal chelator that induces differentiation and apoptosis in teratocarcinoma F9 cells (1), mediated by activation of caspase-3 (2). It also inhibits tyrosinase most likely via metal chelation (3).
Description: The substance Hinokitiol is a iron chelator antioxidant. It is synthetically produced and has a purity of >98%. The pure substance is white solid which is soluble in DMSO or ethanol (25 mg/ml).

Hinokitiol (Iron Chelator antioxidant)

SIH-151-50MG 50 mg
EUR 125
  • Hinokitiol is a natural monoterpenoid. It is a potent metal chelator that induces differentiation and apoptosis in teratocarcinoma F9 cells (1), mediated by activation of caspase-3 (2). It also inhibits tyrosinase most likely via metal chelation (3).
Description: The substance Hinokitiol is a iron chelator antioxidant. It is synthetically produced and has a purity of >98%. The pure substance is white solid which is soluble in DMSO or ethanol (25 mg/ml).