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重组人BMPR1A/BMPR-IA/ALK-3Protein(C-Fc-6His)

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产品名称: 重组人BMPR1A/BMPR-IA/ALK-3Protein(C-Fc-6His)
产品型号: PN100170-10ug
产品展商: PERFEMIKER
产品价格: 400.00 元
会员价格: 0.00 元
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简单介绍

重组人BMPR1A/BMPR-IA/ALK-3Protein(C-Fc-6His) 货号:PN100170 规格:10ug; 标签:C-Fc-6His; 来源:Human; 表达宿主:Human cells


重组人BMPR1A/BMPR-IA/ALK-3Protein(C-Fc-6His)  的详细介绍

名称:重组人BMPR1A/BMPR-IA/ALK-3Protein(C-Fc-6His);


产品说明(Description)
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 Fc, 6His tag at the C-terminus. 
Accession #: P36894
Known as: 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

制剂(Formulation)
Lyophilized from a 0.2 μm filtered solution of PBS, pH 7.4.

质量控制(Quality Control) 
Purity:  Greater than 95% as determined by reducing SDS-PAGE.    
Endotoxin: Less than 0.1 ng/ug (1 IEU/ug) as determined by LAL test.

复溶(Reconstitution)
Always centrifuge tubes before opening. Do not mix by vortex or pipetting.
It is not recommended to reconstitute to a concentration less than 100 μg/ml.
Dissolve the lyophilized protein in ddH2O.
Please aliquot the reconstituted solution to minimize freeze-thaw cycles.    

保存(Storage)
Lyophilized protein should be stored at < -20°C, though stable at room temperature for 3 weeks.Reconstituted protein solution can be stored at 4-7°C for 2-7 days.Aliquots of reconstituted samples are stable at < -20°C for 3 months.    

背景(Background)
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).

电泳(SDS-PAGE)

FOR RESEARCH USE ONLY