Lipin 1 Antibody [G22A22]

Catalog No.: F2643

    Application: Reactivity:
    • Lane 1: 3T3-L1, Lane 2: 3T3-L1 adipocytes (differentiated,7 d)
    1/

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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
    1:100
    1:1600
    Application
    WB, IP, IF
    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
    130 kDa

    Datasheet & SDS

    生物学的記述

    Specificity
    Lipin 1 Antibody [G22A22] detects endogenous levels of total Lipin 1 protein.
    Clone
    G22A22
    Synonym(s)
    Phosphatidate phosphatase LPIN1; Lipin-1; LPIN1; KIAA0188
    Background
    Lipin 1 (LPIN1) belongs to the Lipin family of phosphatidate phosphatase enzymes (PAPs) that regulate lipid metabolism across multiple tissues, including adipose, liver, muscle, and brain. It features an N-terminal nuclear localization domain, a central catalytic Haloacid Dehalogenase (HAD)-like phosphatase domain responsible for Mg²⁺-dependent phosphatidic acid (PA) hydrolysis, and a C-terminal Lipin-specific region with a polybasic motif (K/R-rich sequence) that binds PA and serves as a nuclear localization signal. Key regulatory sites include phosphorylation motifs targeted by AKT1, mTOR, and LKB1, influencing its stability and subcellular shuttling between the nucleus and the endoplasmic reticulum. Lipin 1 exhibits dual roles: as a PAP enzyme, it converts PA to diacylglycerol (DAG) in the Kennedy pathway, driving triglyceride (TG), phosphatidylcholine, and phosphatidylethanolamine synthesis essential for lipid droplet formation and adipogenesis. As a transcriptional coactivator, it interacts with PPARα, PGC-1α, PPARγ, and C/EBPα in the nucleus to upregulate lipogenic and metabolic genes, while reciprocally enhancing PI3K-AKT-mTOR signaling via AKT1 activation. Lipin 1 mutations cause rhabdomyolysis, lipodystrophy with fatty liver, hypertriglyceridemia, insulin resistance, and are implicated in cancer via dysregulated mTOR pathways.
    References

    技術サポート

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