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骨形態發生蛋白15抗體

  • 產品貨號:mlR6612-3 收藏此商品
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產品 :  mlR6612

英文名稱 :  BMP15

中文名稱 :  骨形態發生蛋白15抗體

    :  BMP 15; BMP-15; BMP15; BMP15_HUMAN; Bone morphogenetic protein 15; GDF 9B; GDF-9B; GDF9B; Growth/differentiation factor 9B; ODG2; POF4.  

研究領域 :  心血管  發育生物學  染色質和核信號  信號轉導  干細胞  生長因子和激素  轉錄調節因子  

抗體來源 :  Rabbit

克隆類型 :  Polyclonal

交叉反應 :   Human, Mouse, Rat, Chicken, Pig, Cow, Horse, Rabbit, Sheep,

產品應用 :  WB=1:500-2000 ELISA=1:500-1000  

not yet tested in other applications.

optimal dilutions/concentrations should be determined by the end user.

 :  14kDa

細胞定位 :  分泌型蛋白

    :  Lyophilized or Liquid

    :  1mg/ml

 :  KLH conjugated synthetic peptide derived from human BMP15:321-392/392

    :  IgG

純化方法 :  affinity purified by Protein A

 :  0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

保存條件 :  Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.

PubMed :  PubMed

產品介紹background:

The BMP15 protein is a member of the bone morphogenetic protein family which is part of the transforming growth factor beta superfamily. The transforming growth factor beta superfamily includes large families of growth and differentiation factors. It is thought that BMP15 may be involved in oocyte maturation and follicular development as a homodimer, or by forming heterodimers with a related protein, Gdf9.

Function:

May be involved in follicular development. Oocyte-specific growth/differentiation factor that stimulates folliculogenesis and granulosa cell (GC) growth.

Subunit:

Homodimer. But, in contrast to other members of this family, cannot be disulfide-linked.

Subcellular Location:

Secreted.

DISEASE:

Defects in BMP15 are the cause of ovarian dysgenesis type 2 (ODG2) [MIM:300510]; also known as X-linked hypergonadotropic ovarian dysgenesis or hypergonadotropic ovarian failure due to ovarian dysgenesis. Ovarian dysgenesis leads to ovarian failure and accounts for about half of the cases of primary amenorrhea.

Defects in BMP15 are the cause of premature ovarian failure type 4 (POF4) [MIM:300510]. An ovarian disorder defined as the cessation of ovarian function under the age of 40 years. It is characterized by oligomenorrhea or amenorrhea, in the presence of elevated levels of serum gonadotropins and low estradiol.

Similarity:

Belongs to the TGF-beta family.

SWISS:

O95972

Gene ID:

9210

Important Note:

This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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