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CLIP2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

CLIP2 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 ABIN2712880
发货至: 中国
  • 抗原 See all CLIP2 蛋白
    CLIP2 (CAP-GLY Domain Containing Linker Protein 2 (CLIP2))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 3
    • 1
    资源
    • 2
    • 2
    HEK-293 Cells
    标记
    This CLIP2 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human CLIP2 (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 CLIP2 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
    CLIP2 (CAP-GLY Domain Containing Linker Protein 2 (CLIP2))
    别名
    Clip2 (CLIP2 产品)
    别名
    CLIP Protein, CLIP-115 Protein, CYLN2 Protein, WBSCR3 Protein, WBSCR4 Protein, WSCR3 Protein, WSCR4 Protein, Cyln2 Protein, B230327O20 Protein, Clip1 Protein, mKIAA0291 Protein, wbscr4 Protein, CAP-Gly domain containing linker protein 2 Protein, CAP-GLY domain containing linker protein 2 Protein, CLIP2 Protein, Clip2 Protein, clip2 Protein
    背景
    The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.
    分子量
    115.6 kDa
    NCBI登录号
    NP_003379
    途径
    Microtubule Dynamics
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