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ECM BIOSCIENCES/Cofilin 1 + LIMK1 Phosphorylated/100 μl/CL7321

价格
¥1500.00
货号:CL7321
浏览量:127
品牌:ECM BIOSCIENCES
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商品描述

Members of the ADF/cofilin (AC) family are actin-severing proteins that regulate actin remodeling during cell migration, cytokinesis, axon development, and immune cell activation. In mammals, there are three members of the AC family, muscle-specific cofilin (cofilin 2), non-muscle cofilin (cofilin 1), and ADF. In humans, cofilin 1 and ADF have 72% identity, with the major amino acid differences found in the C-terminal region. Activation of cofilin kinases, LIMK1 or LIMK2, leads to phosphorylation of cofilin at serine 3. This phosphorylation disrupts cofilin binding to actin in vitro and in vivo.

For preparation of Ser-3 phosphorylated Cofilin, purified human Cofilin 1 was phosphorylated in vitro with His-tagged mouse recombinant LIM Kinase 1 for 30 min. at 37°C (Cat. #CL7321). For control lysate, the recombinant Cofilin 1 protein was exposed to buffer only (Cat.#CL7311). The phosphorylated product is detected by anti-Cofilin (Ser-3; Cat.#CP1151), while both the control and phosphorylated recombinant cofilin 1 are detected by anti-Cofilin (N-terminus; Cat.#CP1131).

Cofilin 1 Control Lysate is supplied at a concentration of 10 ng/µl in electrophoresis sample buffer (62.5 mM Tris pH 6.8, 2% SDS, 5% glycerol, 0.003% bromophenol blue, 0.9% β-mercaptoethanol). Store at –20°C. Do not boil or dilute. Stable for 1 year.

The products are are safely shipped at ambient temperature for both domestic and international shipments. Each product is guaranteed to match the specifications as indicated on the corresponding technical data sheet. Please store at -20C upon arrival for long term storage.

*All molecular weights (MW) are confirmed by comparison to Bio-Rad Rainbow Markers and to western blotmobilities of known proteins with similar MW.

This kit contains:

KIT SUMMARY

ECM BIOSCIENCES的A431细胞裂解液A431细胞在细胞表面表达约106种表皮生长因子(EGF)受体。在用EGF刺激后,A431细胞的EGF受体磷酸化水平显着增加,随后激活了主要的细胞信号传导途径,例如PKB / Akt和MAP激酶途径。在EGF刺激后的不同时间点,这些细胞信号通路的下游,各种细胞骨架,细胞质和核蛋白被磷酸化。在含有10%胎牛血清的DMEM中生长的A431细胞的融合培养物在1%SDS,1.0 mM原钒酸钠,10 mM Tris(pH 7.4)缓冲液中裂解。在稀释至最终浓度和缓冲液之前,使用BCA方法(Pierce)确定蛋白质浓度。