research use only

UQCRC2 Antibody [C21D5]

Cat.No.: F5996

    Application: Reactivity:
    • F5996-wb
      Lane 1: HepG2, Lane 2: Huh7, Lane 3: A172, Lane 4: 293T

    Usage Information

    Dilution
    1:1000
    1:50
    Application
    WB, IP
    Reactivity
    Human, Mouse, Rat
    Source
    Rabbit Monoclonal Antibody
    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
    48 kDa

    Datasheet & SDS

    Biological Description

    Specificity
    UQCRC2 Antibody [C21D5] detects endogenous levels of total UQCRC2 protein.
    Clone
    C21D5
    Synonym(s)
    Cytochrome b-c1 complex subunit 2, mitochondrial; Complex III subunit 2; Core protein II; Ubiquinol-cytochrome-c reductase complex core protein 2; UQCRC2
    Background
    UQCRC2 (ubiquinol‑cytochrome c reductase core protein 2) is a nuclear‑encoded structural subunit of the mitochondrial cytochrome b‑c1 complex (Complex III) that is embedded in the inner mitochondrial membrane and contributes to the assembly, stability, and electron‑transport activity of the ubiquinol‑cytochrome c oxidoreductase complex. Within the electron transport chain, UQCRC2‑containing Complex III transfers electrons from ubiquinol to cytochrome c, coupling this redox reaction to proton translocation across the inner membrane and supporting the electrochemical gradient that drives ATP synthesis and mitochondrial integrity. UQCRC2 expression is transcriptionally regulated by AMP‑activated protein kinase (AMPK) through activation of the transcription factor NFE2L2/NRF2, and this AMPK‑NRF2–UQCRC2 axis enhances UQCRC2 levels and promotes mitophagy, the selective clearance of damaged mitochondria, thereby protecting hepatocytes against alcohol‑induced liver injury. UQCRC2 is downregulated in tumor tissue compared with adjacent non‑carcinoma tissue, and its expression correlates inversely with lymph node metastasis, relapse, and tumor grade; UQCRC2 overexpression suppresses gastric cancer cell proliferation, migration, and invasion in vitro and in vivo, whereas reduction of UQCRC2 by upstream miRNAs such as miR‑370 enhances tumor aggressiveness.
    References
    • https://pubmed.ncbi.nlm.nih.gov/33719895/
    • https://pubmed.ncbi.nlm.nih.gov/32742452/

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