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Animal-Free Recombinant Human BMP-13/CDMP-2

类型:细胞因子及添加物
品牌:PeproTech
种属:Human
应用:Functional

规格: 10µg

货号: AF-120-04-10

价格: ¥0.00

规格: 50µg

货号: AF-120-04-50

价格: ¥0.00

规格: 100µg

货号: AF-120-04-100

价格: ¥0.00

规格: 250µg

货号: AF-120-04-250

价格: ¥0.00

规格: 500µg

货号: AF-120-04-500

价格: ¥0.00

规格: 1mg

货号: AF-120-04-1000

价格: ¥0.00

数量:

产品规格

种属

Human

已发表种属

Human

Expression System

E. coli

氨基酸序列

TAFASRHGKR HGKKSRLRCS KKPLHVNFKE LGWDDWIIAP LEYEAYHCEG VCDFPLRSHL EPTNHAIIQT LMNSMDPGST PPSCCVPTKL TPISILYIDA GNNVVYKQYE DMVVESCGCR

分子量

27 kDa

分类

Recombinant

类型

Protein

纯度

≥ 95% by SDS-PAGE gel and HPLC analyses.

内毒素浓度

<0.1 EU/µg

活性

Determined by its ability to induce alkaline phosphatase production by ATDC-5 cells. The expected ED50 for this effect is 2.0-3.0 ug/ml.

偶联物

Unconjugated

形式

Lyophilized

纯化类型

purified

内含物

no preservative

保存条件

-20°C

运输条件

Ambient

 

产品详细信息

Recombinant Human BMP-13/CDMP-2 is a 27.0 kDa homodimeric disulfide-linked protein consisting of two 120 amino acid polypeptide chains.

This product is shipped at ambient temperature. For storage, handling and reconstitution information, please see the lot-specific Certificate of Analysis

 

靶标信息

GDF6 is a growth differentiation factor (GDFs), which are members of the transforming growth factor (TGF) superfamily that is involved in embryonic development and adult tissue homeostasis. Both GDF6 and GDF7 are closely related to GDF5 which has been shown to induce activation of plasminogen activator, thereby inducing angiogenesis. It is predominantly expressed in long bones during fetal embryonic development and is involved in bone formation. In Xenopus, GDF6 is expressed at the edge of the neural plate and within the anterior neural plate including the eye fields. GDF6 is required for normal formation of some bones and joints in the limbs, skull, and axial skeleton. It may regulate patterning of the ectoderm by interacting with bone morphogenetic proteins (BMPs), and control eye development. Mutations in this gene result in colobomata, which are congenital abnormalities in ocular development, and in Klippel-Feil syndrome (KFS), a congenital disorder of spinal segmentation.

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