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LZTFL1 Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-11375

宿主: Rabbit

反应性: H,M,R

应用: WB,IHC

  • 详情
  • Overview

    Synonyms 5530402H04Rik,6130400H19Rik,AI414725,AW048545,BBS17,DKFZp686H2076,FLJ36386,Leucine zipper transcription factor like 1,Leucine zipper transcription factor like protein 1,Leucine zipper transcription factor-like protein 1,LZTFL 1,Lztfl1,Lztfl1 leucine zipper transcription factor-like 1,LZTL1,MGC106871,MGC108960,Putative uncharacterized protein DKFZp686H2076,LZTFL1抗体
    Swissprot Q9NQ48
    Source Rabbit
    Reactivity Human,Mouse,Rat
    Immunogen Recombinant protein of human LZTFL1
    Application WB(Detection kit: E-IR-R304),IHC(Detection kit: E-IR-R213)
    Recommended dilution WB,,1:500-1:2000;IHC,,1:50-1:200;
    Concentration 0.4 mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Cytosol
    Tissue specificity Expressed in prostate, ovary, stomach, pancreas, esophagus, breast, liver, bladder, kidney, thyroid, colon and lung (at protein level). Down-regulated in multiple primary tumors (at protein level). Detected in testis, heart, skeletal muscle, thymus, spleen, small intestine, and peripheral blood leukocytes.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
    Background 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.
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