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LZTFL1 Protein (Myc-DYKDDDDK Tag)

LZTFL1 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 ABIN2725086
发货至: 中国
  • 抗原 See all LZTFL1 蛋白
    LZTFL1 (Leucine Zipper Transcription Factor-Like 1 (LZTFL1))
    蛋白类型
    Recombinant
    宿主
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    资源
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    HEK-293 Cells
    标记
    This LZTFL1 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human LZTFL1 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 LZTFL1 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
    LZTFL1 (Leucine Zipper Transcription Factor-Like 1 (LZTFL1))
    别名
    Lztfl1 (LZTFL1 产品)
    别名
    lztfl1 Protein, MGC53120 Protein, LZTFL1 Protein, DKFZp469B0113 Protein, fb53f12 Protein, wu:fb53f12 Protein, zgc:56268 Protein, BBS17 Protein, 5530402H04Rik Protein, 6130400H19Rik Protein, AI414725 Protein, AW048545 Protein, leucine zipper transcription factor like 1 L homeolog Protein, leucine zipper transcription factor like 1 Protein, leucine zipper transcription factor-like 1 Protein, lztfl1.L Protein, LZTFL1 Protein, lztfl1 Protein, Lztfl1 Protein
    背景
    This gene encodes a ubiquitously expressed protein that localizes to the cytoplasm. This protein interacts with Bardet-Biedl Syndrome (BBS) proteins and, through its interaction with BBS protein complexes, regulates protein trafficking to the ciliary membrane. Nonsense mutations in this gene cause a form of Bardet-Biedl Syndrome a ciliopathy characterized in part by polydactyly, obesity, cognitive impairment, hypogonadism, and kidney failure. This gene may also function as a tumor suppressor possibly by interacting with E-cadherin and the actin cytoskeleton and thereby regulating the transition of epithelial cells to mesenchymal cells. Alternative splicing of this gene results in multiple transcript variants.
    分子量
    34.4 kDa
    NCBI登录号
    NP_065080
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