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Fukutin Protein (FKTN) (Transcript Variant 1) (Myc-DYKDDDDK Tag)

FKTN 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 ABIN2721450
发货至: 中国
  • 抗原 See all Fukutin (FKTN) 蛋白
    Fukutin (FKTN)
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 3
    • 2
    • 1
    资源
    • 2
    • 2
    • 1
    • 1
    HEK-293 Cells
    标记
    This Fukutin protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Fukutin (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 FKTN 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
    Fukutin (FKTN)
    别名
    Fukutin (FKTN 产品)
    别名
    FCMD Protein, fcmd Protein, im:7163166 Protein, zgc:162828 Protein, FKTN Protein, CMD1X Protein, LGMD2M Protein, MDDGA4 Protein, MDDGB4 Protein, MDDGC4 Protein, D830030O17Rik Protein, Fcmd Protein, fukutin Protein, fukutin S homeolog Protein, Fukutin Protein, FKTN Protein, fktn Protein, fktn.S Protein, Bm1_09375 Protein, Bm1_09380 Protein, Bm1_44655 Protein, Fktn Protein
    背景
    The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene.
    分子量
    53.5 kDa
    NCBI登录号
    NP_001073270
    途径
    Regulation of Carbohydrate Metabolic Process
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