ATF-6 Antibody [G8H4]

Catalog No.: F4203

    Application: Reactivity:

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    代表番号: 045-509-1970|電子メール:sales@selleck.co.jp

    使用情報

    Dilution
    1:1000
    1:50
    Application
    WB, IP
    Source
    Rabbit Monoclonal Antibody
    Reactivity
    Human, Mouse
    Storage Buffer
    PBS, pH 7.2+50% Glycerol+0.05% BSA+0.01% NaN3
    Storage (from the date of receipt)
    -20°C (avoid freeze-thaw cycles), 2 years
    Predicted MW
    90-100 kDa

    Datasheet & SDS

    生物学的記述

    Specificity
    ATF-6 (D4Z8V) Rabbit mAb detects endogenous levels of total ATF-6 protein.
    Clone
    G8H4
    Synonym(s)
    Cyclic AMP-dependent transcription factor ATF-6 alpha; cAMP-dependent transcription factor ATF-6 alpha; Activating transcription factor 6 alpha (ATF6-alpha); ATF6
    Background
    ATF-6 (Activating Transcription Factor 6) is a type II transmembrane glycoprotein belonging to the bZIP transcription factor family, residing in the endoplasmic reticulum (ER) membrane as a key sensor of the unfolded protein response (UPR). ATF6 features an N-terminal cytoplasmic domain with a basic leucine zipper (bZIP) DNA-binding motif and transcriptional activation regions facing the cytosol, a single transmembrane helix, and a C-terminal ER luminal domain that associates with BiP/GRP78 under homeostatic conditions. Upon ER stress from unfolded protein accumulation, BiP dissociates from ATF6, enabling its trafficking to the Golgi apparatus for sequential cleavage by site-1 protease (S1P) and site-2 protease (S2P), which liberates the active N-terminal cytoplasmic fragment. This cleaved fragment translocates to the nucleus where it binds ER stress response elements (ERSE) to directly activate transcription of UPR target genes, including GRP78/BiP, GRP94, protein disulfide isomerase (PDI), XBP1, and CHOP, enhancing ER chaperone capacity, protein folding, ER-associated degradation (ERAD), and ER biogenesis to restore proteostasis and promote cell survival. Dysregulation of ATF6 contributes to diabetes through impaired insulin signaling, neurodegeneration via protein aggregation, and cancer progression.
    References

    技術サポート

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