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活性验证

Recombinant Human FGFR-3/JTK4/CD333 (V555M) Protein (RP03332LQ)

Recombinant Human FGFR-3/JTK4/CD333 (V555M) Protein was resolved with SDS-PAGE under reducing (Lane 1) and non-reducing (Lane 2) conditions.

The activity of FGFR3 is based on the MSA technology, and the content and ratio of the substrate and the product are directly separated and detected in real time and dynamically by the different migration rates of the substrate and the product after the enzymatic reaction.

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货号: RP03332LQ
促销价:   ¥2500
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详细信息

种属
Human
表达宿主
Baculovirus-Insect Cells
Calculated MW
62.8 kDa
Observed MW
50-60 kDa
标签
N-His-GST
纯度
> 90% by SDS-PAGE and HPLC
内毒素
< 1.0 EU/μg of the protein by LAL method
制剂
Supplied as a 0.22 μm filtered solution in 50 mM Tris-HCl, 200 mM NaCl, 20% glycerol, 1 mM DTT. (pH 7.5). Contact us for customized product form or formulation.
描述
Recombinant Human FGFR-3/JTK4/CD333 (V555M) Protein is produced by Baculovirus-Insect Cells expression system. The target protein is expressed with sequence (Pro449-Glu759 (V555M)) of Human FGFR3 (Accession #P22607) fused with a N-His-GST tag.
储存
Store at -70°C. This product is stable at ≤ -70°C for up to 1 year from the date of receipt. For optimal storage, aliquot into smaller quantities after centrifugation and store at recommended temperature. 
Aliquots below 10 μL are not advisable. Product must not be stored in diluted solutions. Avoid repeated freeze-thaw cycles.未开盖的干粉蛋白在 -20°C至-80°C可保存12个月;
复溶之后,蛋白溶液在-20°C及以下可保存3个月,在2-8℃可保存1周。
生物活性
The activity of FGFR3 is based on the MSA technology, and the content and ratio of the substrate and the product are directly separated and detected in real time and dynamically by the different migration rates of the substrate and the product after the enzymatic reaction.

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背景信息

FGFR3 also known as CD333 is a member of the fibroblast growth factor receptor (FGFR) family, which includes FGFR1-4, and FGFRL1. FGFR1-4 are cell surface membrane receptors that possess tyrosine kinase activity. FGFR3 plays a role in bone growth by regulating ossification. Gain of function mutations in FGFR3 inhibits chondrocyte proliferation and underlies achondroplasia and hypochondroplasia. FGFR3 inhibitors are in early clinical trials as a cancer treatment, e.g. BGJ398 for urothelial carcinoma. The FGFR3 receptor has a tyrosine kinase signaling pathway that is associated with many biological developments embryonically and in tissues. Studying the tyrosine kinase signaling pathway that FGFR3 displays has played a crucial role in the development of research of several cell activities.

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