Qvd Apexbio

Adrenomedullin (1-12), human
A1001-10 10 mg
EUR 164.4
Description: Adrenomedullin (AM) (1-12), human (C64H100N22O19S1), is a peptide with the sequence Tyr-Arg-Gln-Ser-Met-Asn-Asn-Phe-Gln-Gly-Leu-Arg. It was first discovered to be associated with pheochromocytoma, a tumor arising from adrenal medulla, in 1993.

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

TAK-875
50 mg
EUR 714
Description: TAK-875 is a potent, selective, and oral GPR40 agonist. GPR40 is one of the G protein-coupled receptors predominantly expressed in pancreatic ?-cells, mediating enhancement of glucose-stimulated insulin secretion by free fatty acids.

TAK-875
Evaluation Sample
EUR 97.2
Description: TAK-875 is a potent, selective, and oral GPR40 agonist. GPR40 is one of the G protein-coupled receptors predominantly expressed in pancreatic ?-cells, mediating enhancement of glucose-stimulated insulin secretion by free fatty acids.

Cyclopamine
10 mg
EUR 150
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
25 mg
EUR 199.2
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].

Cyclopamine
5 mg
EUR 129.6
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
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
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].

Human Samples information

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.

PF-562271 HCl
A8345-5.1 10 mM (in 1mL DMSO)
EUR 393.6
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
A8345-50 50 mg
EUR 714
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-S Evaluation Sample
EUR 97.2
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.

BYL-719
A8346-100 100 mg
EUR 1039.2
Description: BYL719 is a selective PI3K? inhibitor with IC50 of 5 nM. It has minimal effect on PI3K?, ? and ?[1]. Dysregulation of the PI3K signaling pathway is involved in multiple cancers.