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CDH23 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)

CDH23 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 ABIN2713021
发货至: 中国
  • 抗原 See all CDH23 蛋白
    CDH23 (Cadherin 23 (CDH23))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 2
    宿主
    • 3
    • 1
    资源
    • 3
    • 1
    HEK-293 Cells
    标记
    This CDH23 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Cadherin-23 (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 CDH23 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
    CDH23 (Cadherin 23 (CDH23))
    别名
    Cadherin-23 (CDH23 产品)
    别名
    4930542A03Rik Protein, USH1D Protein, ahl Protein, ahl1 Protein, bob Protein, bus Protein, mdfw Protein, nmf112 Protein, nmf181 Protein, nmf252 Protein, sals Protein, v Protein, CDHR23 Protein, W Protein, cadherin 23 (otocadherin) Protein, cadherin related 23 Protein, cadherin-related 23 Protein, Cdh23 Protein, CDH23 Protein
    背景
    This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Upregulation of this gene may also be associated with breast cancer. Alternative splice variants encoding different isoforms have been described.
    分子量
    58.4 kDa
    NCBI登录号
    NP_443068
    途径
    Sensory Perception of Sound
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