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Merck
모든 사진(1)

Key Documents

12-151

Sigma-Aldrich

PKA Inhibitor Peptide

lyophilized powder, for Neuroscience applications

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About This Item

UNSPSC 코드:
12352202
eCl@ss:
32160405
NACRES:
NA.41

product name

PKA Inhibitor peptide, The PKA Inhibitor peptide controls the biological activity of PKA. This small molecule/inhibitor is primarily used for Neuroscience applications.

Quality Level

형태

lyophilized powder

제조업체/상표

Upstate®

기술

activity assay: suitable (kinase)

NCBI 수납 번호

UniProt 수납 번호

배송 상태

wet ice

생화학적/생리학적 작용

Protein Target: PKA
Target Sub-Family: AGC

품질

Routinely evaluated by inhibition of PKA catalytic subunit (14-114).

물리적 형태

Lyophilized powder (from H2O)

저장 및 안정성

Lyophilized: Stable for 2 years at -20°C . Rehydrated: Stable for 1 year at -20°C.

법적 정보

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

면책조항

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Heterogeneity in beta-adrenergic receptor kinase expression in the lung accounts for cell-specific desensitization of the beta2-adrenergic receptor
McGraw, D. W. and Liggett, S. B.
The Journal of Biological Chemistry, 272, 7338-7344 (1997)
Y I Lee et al.
The Journal of biological chemistry, 276(20), 16969-16977 (2001-03-30)
The hepatitis B virus-X (HBx) protein is known as a multifunctional protein that not only coactivates transcription of viral and cellular genes but coordinates the balance between proliferation and programmed cell death, by inducing or blocking apoptosis. In this study
Primary structural determinants essential for potent inhibition of cAMP-dependent protein kinase by inhibitory peptides corresponding to the active portion of the heat-stable inhibitor protein.
Glass, D B, et al.
The Journal of Biological Chemistry, 264, 8802-8810 (1989)
H L Lai et al.
The Journal of biological chemistry, 272(8), 4970-4977 (1997-02-21)
We have previously reported that phosphorylation of adenylyl cyclase type VI (AC6) may result in the suppression of adenylyl cyclase activity during desensitization of the A2a-adenosine receptor-mediated cAMP response (A2a desensitization) in rat pheochromocytoma PC12 cells. In the present study

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