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Claudin 19 Protein (CLDN19) (Transcript Variant 2) (Myc-DYKDDDDK Tag)

CLDN19 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 ABIN2712854
发货至: 中国
  • 抗原 See all Claudin 19 (CLDN19) 蛋白
    Claudin 19 (CLDN19)
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 2
    宿主
    • 4
    • 1
    资源
    • 2
    • 2
    • 1
    HEK-293 Cells
    标记
    This Claudin 19 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Claudin-19 / CLDN19 (transcript variant 2) 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 CLDN19 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
    Claudin 19 (CLDN19)
    别名
    Claudin-19,cldn19 (CLDN19 产品)
    别名
    HOMG5 Protein, claudin-19 Protein, zgc:112141 Protein, claudin 19 Protein, claudin 19 S homeolog Protein, CLDN19 Protein, Cldn19 Protein, cldn19.S Protein, cldn19 Protein
    背景
    The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene.
    分子量
    21.9 kDa
    NCBI登录号
    NP_001116867
    途径
    Cell-Cell Junction Organization, Hepatitis C
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