Apexbio A8524

Sodium Orthovanadate

A8524-25000 25 g
EUR 268.8
Description: Sodium orthovanadate is a commonly used general inhibitor for PTP (protein tyrosine phosphatases), alkaline phosphatase (ALP) and ATPase. Na3VO4 acts as a competitive inhibitor and is completely reversible upon the addition of EDTA or by dilution.

Apexbio Reagents Laboratories manufactures the apexbio a8524 reagents distributed by Genprice. The Apexbio A8524 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 Apexbio Reagents. Other Apexbio products are available in stock. Specificity: Apexbio Category: A8524

Human Samples information

Cyclopamine

A8340-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: Cyclopamine is a naturally occurring Hedgehog (Hh)?specific small?molecule signaling steroidal alkaloid inhibitor, causes a profound inhibition of tumor growth, has significant anti?invasive, anti?proliferative and anti?estrogenic potency in human breast cancer cells [2] [1].

Cyclopamine

A8340-S Evaluation Sample
EUR 97.2
Description: Cyclopamine is a naturally occurring Hedgehog (Hh)?specific small?molecule signaling steroidal alkaloid inhibitor, causes a profound inhibition of tumor growth, has significant anti?invasive, anti?proliferative and anti?estrogenic potency in human breast cancer cells [2] [1].

Go 6976

A8341-1 1 mg
EUR 172.8
Description: Go 6976 is a selective inhibitor of PKC with IC50 value of 20 nM [1] [2].

Go 6976

A8341-5 5 mg
EUR 348
Description: Go 6976 is a selective inhibitor of PKC with IC50 value of 20 nM [1] [2].

GF 109203X

A8342-10 10 mg
EUR 226.8
Description: GF 109203X is a potent and selective inhibitor of protein kinase C [1].

GF 109203X

A8342-5 5 mg
EUR 142.8
Description: GF 109203X is a potent and selective inhibitor of protein kinase C [1].

GF 109203X

A8342-5.1 10 mM (in 1mL DMSO)
EUR 199.2
Description: GF 109203X is a potent and selective inhibitor of protein kinase C [1].

GF 109203X

A8342-S Evaluation Sample
EUR 97.2
Description: GF 109203X is a potent and selective inhibitor of protein kinase C [1].

Go 6983

A8343-10 10 mg
EUR 247.2
Description: Go 6983 is a selective inhibitor of PKC?, PKC?, PKC?, PKC? and PKC? with IC50 value of 7 nM, 7 nM, 6 nM, 10 nM, and 20 mM, respectively [1].

Go 6983

A8343-5 5 mg
EUR 177.6
Description: Go 6983 is a selective inhibitor of PKC?, PKC?, PKC?, PKC? and PKC? with IC50 value of 7 nM, 7 nM, 6 nM, 10 nM, and 20 mM, respectively [1].

Go 6983

A8343-5.1 10 mM (in 1mL DMSO)
EUR 199.2
Description: Go 6983 is a selective inhibitor of PKC?, PKC?, PKC?, PKC? and PKC? with IC50 value of 7 nM, 7 nM, 6 nM, 10 nM, and 20 mM, respectively [1].

K-252c

A8344-1 1 mg
EUR 204
Description: K-252c is a cell-permeable, reversible, and ATP-competitive inhibitor of protein kinase C (PKC) and protein kinase A (PKA) with IC50 value of 2.45 ?M and 25.7 ?M, respectively.

K-252c

A8344-25 25 mg
EUR 1452
Description: K-252c is a cell-permeable, reversible, and ATP-competitive inhibitor of protein kinase C (PKC) and protein kinase A (PKA) with IC50 value of 2.45 ?M and 25.7 ?M, respectively.

K-252c

A8344-5 5 mg
EUR 616.8
Description: K-252c is a cell-permeable, reversible, and ATP-competitive inhibitor of protein kinase C (PKC) and protein kinase A (PKA) with IC50 value of 2.45 ?M and 25.7 ?M, respectively.

K-252c

A8344-5.1 10 mM (in 1mL DMSO)
EUR 518.4
Description: K-252c is a cell-permeable, reversible, and ATP-competitive inhibitor of protein kinase C (PKC) and protein kinase A (PKA) with IC50 value of 2.45 ?M and 25.7 ?M, respectively.

PF-562271 HCl

A8345-10 10 mg
EUR 324
Description: PF-562271 is a potent, ATP-competitive and reversible inhibitor of both focal adhesion kinase (FAK), a non-receptor tyrosine kinase involved in a variety of cellular events, and proline-rich tyrosine kinase 2 (Pyk2), an FAK homolog containing 48% amino acid identity.

PF-562271 HCl

A8345-5 5 mg
EUR 226.8
Description: PF-562271 is a potent, ATP-competitive and reversible inhibitor of both focal adhesion kinase (FAK), a non-receptor tyrosine kinase involved in a variety of cellular events, and proline-rich tyrosine kinase 2 (Pyk2), an FAK homolog containing 48% amino acid identity.