Recombinant Human BMPR1A (C-Fc-6His)

Recombinant Human BMPR1A (C-Fc-6His)

规格:10µg      价格:¥360
规格:50µg      价格:¥1080
规格:500µg    价格:¥8000
SKU: PHH0160 Category: 靶点蛋白 Tags: , ,

说明书 复制

产品名称

Recombinant Human BMPR1A (C-Fc-6His)

英文名称

ALK-3/BMPR1A/BMPR-IA  

纯度

Greater than 95% as determined by reducing SDS-PAGE

内毒素

<1 EU/µg as determined by LAL test.

蛋白构建

Recombinant Human Bone Morphogenetic Protein Receptor Type IA/Activin Receptor-like Kinase 3 is produced by our Mammalian expression system and the target gene encoding Gln24-Arg152 is expressed with a human IgG1 Fc, 6His tag at the C-terminus.

Accession

P36894

表达宿主

Human Cells

种属

Human

预测分子量

42.1 KDa

制剂

Lyophilized from a 0.2 μm filtered solution of PBS, pH 7.4.

运输方式

The product is shipped at ambient temperature.Upon receipt, store it immediately at the temperature listed below.

稳定性&储存

Store at ≤-70°C, stable for 6 months after receipt.Store at ≤-70°C, stable for 3 months under sterile conditions after opening. Please minimize freeze-thaw cycles.

复溶

Always centrifuge tubes before opening.Do not mix by vortex or pipetting.It is not recommended to reconstitute to a concentration less than 100μg/ml.Dissolve the lyophilized protein in distilled water.Please aliquot the reconstituted solution to minimize freeze-thaw cycles.

 

分子别名
Bone Morphogenetic Protein Receptor Type-1A; BMP Type-1A Receptor; BMPR-1A; Activin Receptor-Like Kinase 3; ALK-3; Serine/Threonine-Protein Kinase Receptor R5; SKR5; CD292; BMPR1A; ACVRLK3; ALK3

 

背景介绍
Bone Morphogenetic Protein Receptor Type-1A (BMPR1A) belongs to the TKL Ser/Thr protein kinase family and TGFB receptor subfamily, including the type I receptors BMPR1A and BMPR1B and the type II receptor BMPR2. BMPR1A is a single-pass type I membrane protein and highly expressed in skeletal muscle. BMPR1A contains one GS domain and one protein protein kinase domain. BMPR1A is necessary for the extracellular matrix depostition by osteoblasts. BMPR1A can activate SMAD transcriptional regulators, binding with ligands. Defects in BMPR1A are a cause of juvenile polyposis syndrome, Cowden disease and hereditary mixed polyposis syndrome 2 (HMPS2).

 

注意事项

本司产品仅用于科研,不用于临床诊断和治疗

 


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