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FAM65B Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)

FAM65B 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 ABIN2720801
发货至: 中国
  • 抗原 See all FAM65B 蛋白
    FAM65B (Family with Sequence Similarity 65, Member B (FAM65B))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 2
    宿主
    • 2
    • 1
    资源
    • 2
    • 1
    HEK-293 Cells
    标记
    This FAM65B protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human FAM65B (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 FAM65B 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
    FAM65B (Family with Sequence Similarity 65, Member B (FAM65B))
    别名
    Fam65b (FAM65B 产品)
    别名
    C6orf32 Protein, DIFF40 Protein, DIFF48 Protein, MYONAP Protein, PL48 Protein, 1700108N18Rik Protein, 6330500D04Rik Protein, AI225904 Protein, E430013J17Rik Protein, si:dkey-218n20.1 Protein, Ab2-162 Protein, RGD1306939 Protein, RHO family interacting cell polarization regulator 2 Protein, family with sequence similarity 65, member B Protein, ripor2 Protein, RIPOR2 Protein, Ripor2 Protein, FAM65B Protein
    背景
    This gene encodes an atypical inhibitor of the small G protein RhoA. Inhibition of RhoA activity by the encoded protein mediates myoblast fusion and polarization of T cells and neutrophils. The encoded protein is a component of hair cell stereocilia that is essential for hearing. A splice site mutation in this gene results in hearing loss in human patients.
    分子量
    65.5 kDa
    NCBI登录号
    NP_056948
    途径
    Transition Metal Ion Homeostasis
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