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CD42b/GP1BA Protein, Human, Recombinant (aa 17-531, His)

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CD42b/GP1BA Protein, Human, Recombinant (aa 17-531, His)
产品编号 TMPY-05034U

CD42b/GP1BA Protein, Human, Recombinant (aa 17-531, His) is expressed in HEK293 Cells. The accession number is P07359.

CD42b/GP1BA Protein, Human, Recombinant (aa 17-531, His)

CD42b/GP1BA Protein, Human, Recombinant (aa 17-531, His)

一键复制产品信息
SPR兼容缓冲液
CD42b/GP1BA Protein, Human, Recombinant (aa 17-531, His)
产品编号 TMPY-05034U
CD42b/GP1BA Protein, Human, Recombinant (aa 17-531, His) is expressed in HEK293 Cells. The accession number is P07359.
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产品信息

生物活性
Immobilized Human CD42b, His Tag at 0.5 μg/ml (100 μl/well) on the plate. Dose response curve for Anti-CD42b Antibody, hFc Tag with the EC50 of 4.0 ng/ml determined by ELISA.
产品描述
CD42b/GP1BA Protein, Human, Recombinant (aa 17-531, His) is expressed in HEK293 Cells. The accession number is P07359.
种属
Human
表达系统
HEK293 Cells
标签C-His
蛋白编号P07359
别名
VWDP,GPIbα,GPIbalpha,GPIbA,GP1B,glycoprotein Ib (platelet), α polypeptide,glycoprotein Ib (platelet), alpha polypeptide,DBPLT3,CD42b-α,CD42b-alpha,CD42B,BSS,BDPLT3,BDPLT1
蛋白构建
His17-Leu531
蛋白纯度
> 95% as determined by Tris-Bis PAGE; > 95% as determined by HPLC
分子量57.6 kDa (Predicted); 110-115 kDa (Due to glycosylation)
内毒素< 1.0 EU/μg of the protein as determined by the LAL method.
蛋白性状Lyophilized powder
缓冲液Lyophilized from 0.22 μm filtered solution in PBS (pH 7.4). Normally 8% trehalose is added as protectant before lyophilization.
存储
Lyophilized powders can be stably stored for over 12 months, while liquid products can be stored for 6-12 months at -80°C. For reconstituted protein solutions, the solution can be stored at -20°C to -80°C for at least 3 months. Please avoid multiple freeze-thaw cycles and store products in aliquots.
运输方式In general, Lyophilized powders are shipping with blue ice. Solutions are shipping with dry ice.
研究背景
Absence of the CD42 complex leads to the Bernard-Soulier syndrome (BSS), which is a bleeding disorder characterized by thrombocytopenia and giant platelets. So far, mutations have been found in the genes encoding CD42a, CD42b and CD42c in patients with BSS**.

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