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LZTFL1 抗体

LZTFL1 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7237342
发货至: 中国
  • 抗原 See all LZTFL1 抗体
    LZTFL1 (Leucine Zipper Transcription Factor-Like 1 (LZTFL1))
    适用
    • 41
    • 19
    • 18
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 51
    • 6
    克隆类型
    • 52
    • 4
    多克隆
    标记
    • 23
    • 5
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    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
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    • 1
    • 1
    • 1
    • 1
    • 1
    This LZTFL1 antibody is un-conjugated
    应用范围
    • 46
    • 25
    • 13
    • 13
    • 6
    • 4
    • 4
    • 3
    • 3
    • 3
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human LZTFL1
    亚型
    IgG
    Top Product
    Discover our top product LZTFL1 Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.4 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    LZTFL1 (Leucine Zipper Transcription Factor-Like 1 (LZTFL1))
    别名
    LZTFL1 (LZTFL1 产品)
    别名
    lztfl1 antibody, MGC53120 antibody, LZTFL1 antibody, DKFZp469B0113 antibody, fb53f12 antibody, wu:fb53f12 antibody, zgc:56268 antibody, BBS17 antibody, 5530402H04Rik antibody, 6130400H19Rik antibody, AI414725 antibody, AW048545 antibody, leucine zipper transcription factor like 1 L homeolog antibody, leucine zipper transcription factor like 1 antibody, leucine zipper transcription factor-like 1 antibody, lztfl1.L antibody, LZTFL1 antibody, lztfl1 antibody, Lztfl1 antibody
    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
    35 kDa
    UniProt
    Q9NQ48
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