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Merck
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Key Documents

12-151

Sigma-Aldrich

PKA Inhibitor Peptide

lyophilized powder, for Neuroscience applications

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About This Item

分類程式碼代碼:
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.

品質等級

形狀

lyophilized powder

製造商/商標名

Upstate®

技術

activity assay: suitable (kinase)

UniProt登錄號

運輸包裝

wet ice

生化/生理作用

Protein Target: PKA
Target Sub-Family: AGC

品質

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

外觀

Lyophilized powder (from H2O)

儲存和穩定性

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

法律資訊

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

免責聲明

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.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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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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