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TJP2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

TJP2 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2733788
发货至: 中国
  • 抗原 See all TJP2 蛋白
    TJP2 (Tight Junction Protein 2 (Zona Occludens 2) (TJP2))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    资源
    • 1
    • 1
    • 1
    HEK-293 Cells
    标记
    This TJP2 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human TJP2 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product TJP2 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    TJP2 (Tight Junction Protein 2 (Zona Occludens 2) (TJP2))
    别名
    Tjp2 (TJP2 产品)
    别名
    C9DUPq21.11 Protein, DFNA51 Protein, DUP9q21.11 Protein, X104 Protein, ZO2 Protein, ZO-2 Protein, zo2 Protein, tjp2 Protein, x104 Protein, zo-2 Protein, wu:fb62b09 Protein, zgc:92094 Protein, tight junction protein 2 Protein, tight junction protein 2 L homeolog Protein, tight junction protein 2b (zona occludens 2) Protein, TJP2 Protein, Tjp2 Protein, tjp2.L Protein, tjp2b Protein
    背景
    This gene encodes a zonula occluden that is a member of the membrane-associated guanylate kinase homolog family. The encoded protein functions as a component of the tight junction barrier in epithelial and endothelial cells and is necessary for proper assembly of tight junctions. Mutations in this gene have been identified in patients with hypercholanemia, and genomic duplication of a 270 kb region including this gene causes autosomal dominant deafness-51. Alternatively spliced transcripts encoding multiple isoforms have been observed for this gene.
    分子量
    133.8 kDa
    NCBI登录号
    NP_004808
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