BLNK Monoclonal Antibody

    • 货号:YM0068
    • 应用:WB;IHC;IF;FCM;ELISA
    • 种属:Human;Mouse
      • 靶点:
      • BLNK
      • 简介:
      • >>NF-kappa B signaling pathway;>>Osteoclast differentiation;>>B cell receptor signaling pathway;>>Epstein-Barr virus infection;>>Primary immunodeficiency
      • 基因名称:
      • BLNK
      • 蛋白名称:
      • B-cell linker protein
      • Human Swiss Prot No:
      • Q8WV28
      • Mouse Swiss Prot No:
      • Q9QUN3
      • 免疫原:
      • Purified recombinant fragment of human BLNK expressed in E. Coli.
      • 特异性:
      • BLNK Monoclonal Antibody detects endogenous levels of BLNK protein.
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Monoclonal, Mouse
      • 稀释:
      • WB 1:500 - 1:2000. IHC 1:200 - 1:1000. IF 1:200 - 1:1000. Flow cytometry: 1:200 - 1:400. ELISA: 1:10000. Not yet tested in other applications.
      • 纯化工艺:
      • Affinity purification
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 其他名称:
      • BLNK;BASH;SLP65;B-cell linker protein;B-cell adapter containing a SH2 domain protein;B-cell adapter containing a Src homology 2 domain protein;Cytoplasmic adapter protein;Src homology 2 domain-containing leukocyte protein of 65 kDa;
      • 分子量:
      • 50kD
      • 背景:
      • This gene encodes a cytoplasmic linker or adaptor protein that plays a critical role in B cell development. This protein bridges B cell receptor-associated kinase activation with downstream signaling pathways, thereby affecting various biological functions. The phosphorylation of five tyrosine residues is necessary for this protein to nucleate distinct signaling effectors following B cell receptor activation. Mutations in this gene cause hypoglobulinemia and absent B cells, a disease in which the pro- to pre-B-cell transition is developmentally blocked. Deficiency in this protein has also been shown in some cases of pre-B acute lymphoblastic leukemia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012],
      • 功能:
      • disease:Defects in BLNK are the cause of hypoglobulinemia and absent B-cells [MIM:604515]. This is a developmental blockage at the pro- to pre-B-cell transition.,disease:In 6 of 34 childhood pre-B acute lymphoblastic leukemia (ALL) samples that were tested showed a complete loss or drastic reduction of BLNK expression.,function:Functions as a central linker protein that bridges kinases associated with the B-cell receptor (BCR) with a multitude of signaling pathways, regulating biological outcomes of B-cell function and development. Plays a role in the activation of ERK/EPHB2, MAP kinase p38 and JNK. Modulates AP1 activation. Important for the activation of NF-kappa-B and NFAT. Plays an important role in BCR-mediated PLCG1 and PLCG2 activation and Ca(2+) mobilization and is required for trafficking of the BCR to late endosomes. However, does not seem to be required for pre-BCR-mediated ac
      • 细胞定位:
      • Cytoplasm . Cell membrane . BCR activation results in the translocation to membrane fraction.
      • 组织表达:
      • Expressed in B-cell lineage and fibroblast cell lines (at protein level). Highest levels of expression in the spleen, with lower levels in the liver, kidney, pancreas, small intestines and colon.
      • 产品图片
      • Western Blot analysis using BLNK Monoclonal Antibody against NIH/3T3 (1) and BCBL-1 (2) cell lysate.
      • Immunohistochemistry analysis of paraffin-embedded human cervical cancer tissues with DAB staining using BLNK Monoclonal Antibody.
      • Immunofluorescence analysis of HepG2 cells using BLNK Monoclonal Antibody (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.
      • Flow cytometric analysis of NIH/3T3 cells using BLNK Monoclonal Antibody (green) and negative control (purple).