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Kelch-like protein 41 (KLHL41) protein (Myc-DYKDDDDK Tag)

KLHL41 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 ABIN2723997
发货至: 中国
  • 抗原 See all Kelch-like protein 41 (KLHL41) 蛋白
    Kelch-like protein 41 (KLHL41)
    蛋白类型
    Recombinant
    宿主
    • 4
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    资源
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    HEK-293 Cells
    标记
    Myc-DYKDDDDK Tag
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human KBTBD10 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 KLHL41 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
    Kelch-like protein 41 (KLHL41)
    别名
    Kbtbd10 (KLHL41 产品)
    别名
    Gm112 Protein, Kbtbd10 Protein, SARCOSIN Protein, Krp1 Protein, Sarcosin Protein, KBTBD10 Protein, kbtbd10 Protein, klhl41 Protein, cb52 Protein, kbtbd10b Protein, sarcosin Protein, sb:cb52 Protein, wu:fb24f05 Protein, wu:fc15e07 Protein, kelch-like 41 Protein, kelch-like family member 41 Protein, kelch like family member 41 Protein, kelch like family member 41 L homeolog Protein, kelch-like family member 41b Protein, Klhl41 Protein, KLHL41 Protein, klhl41.L Protein, klhl41b Protein
    背景
    This gene is a member of the kelch-like family. The encoded protein contains a BACK domain, a BTB/POZ domain, and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM), a rare congenital muscle disorder.
    分子量
    67.9 kDa
    NCBI登录号
    NP_006054
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