Phospho-Src Family (Tyr416) Antibody [D13C8]

Catalog No.: F4136

    Application: Reactivity:
    • Lane 1: C6, Lane 2: C6 (Pervanadate, 0.5 mM, 37℃, 40 min)
    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
    Application
    WB, IP
    Source
    Rabbit Monoclonal Antibody
    Reactivity
    Human, Mouse, Rat
    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
    60 kDa

    Datasheet & SDS

    生物学的記述

    Specificity
    Phospho-Src Family (Tyr416) Antibody [D13C8] detects endogenous levels of total Src protein only when it is phosphorylated at Tyr416.
    Clone
    D13C8
    Synonym(s)
    Proto-oncogene tyrosine-protein kinase Src; Proto-oncogene c-Src; pp60c-src (p60-Src); SRC; SRC1
    Background
    Phospho-Src Family (Tyr416) designates the activated state of Src family kinases (SFKs), including Src, Lyn, Fyn, Yes, Lck, Blk, and Hck, non-receptor tyrosine kinases that regulate cell growth, differentiation, survival, and signal transduction from cell surface receptors. SFKs share a conserved architecture with an N-terminal myristoylation site for membrane anchoring, a unique domain, SH3 and SH2 domains for protein and phosphotyrosine interactions, and a C-terminal kinase (SH1) domain containing the activation loop with Tyr416 (Tyr419 in human Src). Phosphorylation at Tyr416, typically through intermolecular autophosphorylation, stabilizes the activation loop in an open, catalytically active conformation, boosting kinase activity by up to 20-fold and driving downstream substrate phosphorylation. This activating phosphorylation is counterbalanced by inhibitory phosphorylation at the C-terminal Tyr530 (Tyr527 in chicken), which promotes intramolecular SH2 binding and an inactive kinase state; dephosphorylation of Tyr530 and phosphorylation of Tyr416 together switch SFKs to their active form. In this state, phospho-Src Family (Tyr416) kinases mediate diverse cellular processes, including proliferation, cytoskeletal rearrangement for migration and adhesion, immune signaling (such as T-cell activation via Lck), and apoptosis regulation, while persistent activation through dysregulation contributes to cancer progression and sustained oncogenic signaling.
    References

    技術サポート

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