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您当前的位置:首页 > 抗体 > Membrin蛋白抗体

Membrin蛋白抗体

  • 产品货号:mlR18786-1 收藏此商品
  • 销售价:1580.00-2480.00
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产品 :  mlR18786

英文名称 :  Membrin

中文名称 :  Membrin蛋白抗体

    :  2310032N09Rik; 27 kDa Golgi SNARE protein; Bos1; EPM6; Golgi SNAP receptor complex member 2; Golgi SNARE; Gosr2; GOSR2_HUMAN; Gs27; Membrin; SNARE.  

研究领域 :  细胞生物  信号转导  

抗体来源 :  Rabbit

克隆类型 :  Polyclonal

交叉反应 :  Human, Mouse, Rat, Pig, Cow, Horse, Rabbit,

产品应用 :  ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.

:  25kDa

细胞定位 :  细胞浆

    :  Lyophilized or Liquid

    :  1mg/ml

:  KLH conjugated synthetic peptide derived from human Membrin:101-200/212

    :  IgG

纯化方法 :  affinity purified by Protein A

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

保存条件 :  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

产品介绍 :   This gene encodes a trafficking membrane protein which transports proteins among the medial- and trans-Golgi compartments. Due to its chromosomal location and trafficking function, this gene may be involved in familial essential hypertension. Three transcript variants encoding three different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Function:

Involved in transport of proteins from the cis/medial-Golgi to the trans-Golgi network.

Subcellular Location:

Golgi apparatus membrane.

DISEASE:

Epilepsy, progressive myoclonic 6 (EPM6) [MIM:614018]: A neurologic disorder characterized by onset of ataxia in the first years of life, followed by action myoclonus and seizures later in childhood, and loss of independent ambulation in the second decade. Cognition is not usually affected, although mild memory difficulties may occur in the third decade.

Similarity:

Belongs to the GOSR2 family.

SWISS:

O14653

Gene ID:

9570

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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