A1006 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 a1006 apexbio reagents distributed by Genprice. The A1006 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 A1006 products are available in stock. Specificity: A1006 Category: Apexbio

Amyloid Precursor C-Terminal Peptide
1 mg
EUR 135.6
Description: Amyloid precursor c-terminal peptide (APP) (C86H118N20O27S) has the amino acid sequence Gly-Tyr-Glu-Asn-Pro-Thr-Tyr-Lys-Phe-Phe-Glu-Gln-Met-Gln-Asn. Although it has been implicated as a regulator of synapse formation, neural plasticity and iron export, the primary function of APP is not known.

Amyloid Precursor C-Terminal Peptide
10 mg
EUR 442.8
Description: Amyloid precursor c-terminal peptide (APP) (C86H118N20O27S) has the amino acid sequence Gly-Tyr-Glu-Asn-Pro-Thr-Tyr-Lys-Phe-Phe-Glu-Gln-Met-Gln-Asn. Although it has been implicated as a regulator of synapse formation, neural plasticity and iron export, the primary function of APP is not known.

Amyloid Precursor C-Terminal Peptide
25 mg
EUR 595.2
Description: Amyloid precursor c-terminal peptide (APP) (C86H118N20O27S) has the amino acid sequence Gly-Tyr-Glu-Asn-Pro-Thr-Tyr-Lys-Phe-Phe-Glu-Gln-Met-Gln-Asn. Although it has been implicated as a regulator of synapse formation, neural plasticity and iron export, the primary function of APP is not known.

Amyloid Precursor C-Terminal Peptide
5 mg
EUR 289.2
Description: Amyloid precursor c-terminal peptide (APP) (C86H118N20O27S) has the amino acid sequence Gly-Tyr-Glu-Asn-Pro-Thr-Tyr-Lys-Phe-Phe-Glu-Gln-Met-Gln-Asn. Although it has been implicated as a regulator of synapse formation, neural plasticity and iron export, the primary function of APP is not known.

Beta-Sheet Breaker Peptide iA?5
10 mg
EUR 164.4
Description: Beta-Sheet Breaker Peptide iA?5 (C33H43N5O8), with the sequence H-Leu-Pro-Phe-Phe-Asp-OH, has been shown to inhibit amyloidogenesis in rat brain models.

Beta-Sheet Breaker Peptide iA?5
25 mg
EUR 205.2
Description: Beta-Sheet Breaker Peptide iA?5 (C33H43N5O8), with the sequence H-Leu-Pro-Phe-Phe-Asp-OH, has been shown to inhibit amyloidogenesis in rat brain models.

Beta-Sheet Breaker Peptide iA?5
5 mg
EUR 122.4
Description: Beta-Sheet Breaker Peptide iA?5 (C33H43N5O8), with the sequence H-Leu-Pro-Phe-Phe-Asp-OH, has been shown to inhibit amyloidogenesis in rat brain models.

Human Samples information

Cyclopamine
A8340-5 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
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.