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CALP2
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
CAS NO:261969-04-4

CALP2 是一种钙调蛋白 (CaM) 拮抗剂 (Kd为 7.9 μM),以亲和力结合CaMEF-hand/Ca2+结合位点。CALP2 抑制CaM依赖性磷酸二酯酶 (phosphodiesterase) 活性并增加细胞内 Ca2+浓度。CALP2 有效抑制粘附和脱粒。CALP2 还是肺泡巨噬细胞的强激活剂。
生物活性

CALP2 is acalmodulin(CaM)antagonist ( (Kdof 7.9 μM)) with high affinity for binding to theCaMEF-hand/Ca2+-binding site. CALP2 inhibitsCaM-dependentphosphodiesteraseactivity and increases intracellular Ca2+concentrations. CALP2 potently inhibits of adhesion and degranulation. CALP2 is also a strong activator of alveolar macrophages[1][2][3][4].

分子量

1357.70

Formula

C68H104N14O13S

CAS 号

261969-04-4

Sequence

Val-Lys-Phe-Gly-Val-Gly-Phe-Lys-Val-Met-Val-Phe

Sequence Shortening

VKFGVGFKVMVF

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

 
 
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