GMP Recombinant Human FGF-10/KGF2

GMP Recombinant Human FGF-10/KGF2

规格:10μg 价格:¥720
规格:50μg 价格:¥2600
规格:100μg 价格:¥4800
SKU: PCH90007 Category: GMP细胞因子 Tags: , ,

说明书 复制

产品名称

GMP Recombinant Human FGF-10/KGF2

蛋白名

FGF-10/KGF2

纯度

Greater than 95% as determined by reducing SDS-PAGE

内毒素

≤10 EU/mg

蛋白构建

Recombinant Human FGF-10/KGF2 is produced by our Mammalian cell expression system and the target gene encoding Gln38-Ser208 is expressed.

Accession #

O15520

蛋白标签

Tag free

表达宿主

Mammalian cell

种属

Human

预测分子量

19.3 kDa

蛋白形态

Lyophilized

储存缓冲液

PBS,5% mannitol and 0.01% Tween 80, pH7.4

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

36 months at -20°C to -80°C in lyophilized state.6 months at -20°C to -80°C under sterile conditions after reconstitution.7-10 days at 2°C to 8°C under sterile conditions after reconstitution.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

Fibroblast growth factor 10;FGF-10;Keratinocyte growth factor 2;FGF10;KGF-2;KGF2

 

蛋白活性

The ED50 for this effect is ≤10 ng/mL.

 

背景介绍

Fibroblast growth factor 10 (FGF-10, KGF-2), is a member of the fibroblast growth factor (FGF) family that includes FGF-3, -7, and -22. KGF-2 is secreted by mesenchymal cells and associates with extracellular FGF-BP. It preferentially binds and activates epithelial cell FGFR2 and interacts more weakly with FGFR1. It plays an important role in the regulation of embryonic development, cell proliferation and cell differentiation. It exhibits mitogenic activity for keratinizing epidermal cells, but essentially no activity for fibroblasts, which is similar to the biological activity of FGF7. FGF10 is required for normal branching morphogenesis. Defects in FGF10 are the cause of autosomal dominant aplasia of lacrimal and salivary glands (ALSG). ALSG has variable expressivity, and affected individuals may have aplasia or hypoplasia of the lacrimal, parotid, submandibular and sublingual glands and absence of the lacrimal puncta. The disorder is characterized by irritable eyes, recurrent eye infections, epiphora (constant tearing) and xerostomia (dryness of the mouth), which increases the risk of dental erosion, dental caries, periodontal disease and oral infections.

 

 


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