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您当前的位置:首页 > 抗体 > 神经元钙结合相关蛋白EFCBP1抗体

神经元钙结合相关蛋白EFCBP1抗体

  • 产品货号:mlR11978-1 收藏此商品
  • 销售价:1580.00-2480.00
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产品货号 :  mlR11978

英文名称 :  NECAB1

中文名称 :  神经元钙结合相关蛋白EFCBP1抗体

   :  EF-CBP1; EF-hand calcium-binding protein 1; EFCBP1; N-terminal EF-hand calcium-binding protein 1; NECA1_HUMAN; Necab1; Neuronal calcium-binding protein 1; STIP-1.  

研究领域 :  细胞生物  神经生物学  信号转导  结合蛋白  

抗体来源 :  Rabbit

克隆类型 :  Polyclonal

交叉反应 :   Human, Mouse, Rat, Dog, Pig, 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.

 :  41kDa

细胞定位 :  细胞浆

    :  Lyophilized or Liquid

    :  1mg/ml

 :  KLH conjugated synthetic peptide derived from human NECAB1/EF-CBP1:51-150/351

    :  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 :   Members of the EF-CBP (N-terminal EF-hand calcium binding protein)/NECAB (neuronal calcium-binding protein) family participate in neuronal calcium signaling. EF-CBP1 (N-terminal EF-hand calcium binding protein 1), also known as STIP-1 or neuronal calcium-binding protein 1 (NECAB1), is a 351 amino acid cytoplasmic protein that contains one antibiotic biosynthesis monooxygenase (ABM) domain and two EF-hand domains. Expressed in brain, EF-CBP1 interacts with copine 6 and Syntaxin, and exists as two alternatively spliced isoforms. The gene encoding EF-CBP1 maps to human chromosome 8, which consists of nearly 146 million base pairs, encodes over 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.

Function:

Expressed in brain (at protein level).

Subcellular Location:

Cytoplasm.

Tissue Specificity:

Expressed in brain

Similarity:

Contains 1 ABM domain.

Contains 2 EF-hand domains.

SWISS:

Q8N987

Gene ID:

64168

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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