smooth muscle Myosin heavy chain 11 Antibody [J22F5]

Catalog No.: F2948

    Application: Reactivity:
    • Lane 1: Human testis
    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 - 1:10000
    1:1000
    1:50
    1:20
    Application
    WB, IHC, IF, FCM
    Source
    Rabbit Monoclonal Antibody
    Reactivity
    Human
    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 Observed MW
    227 kDa 227 kDa
    *なぜ予測分子量と実際の分子量が異なるのか?
    下記の原因により、実際の分子量が予測と異なる:タンパク質の翻訳後修飾(リン酸化/糖鎖付加),スプライシングバリアント,イソフォーム,相対的な電荷,ポリマー。

    Datasheet & SDS

    生物学的記述

    Specificity
    Smooth muscle Myosin heavy chain 11 Antibody [J22F5] detects endogenous levels of total smooth muscle Myosin heavy chain 11 protein.
    Clone
    J22F5
    Synonym(s)
    KIAA0866; MYH11; Myosin-11; Myosin heavy chain 11; SMMHC
    Background
    Smooth muscle myosin heavy chain 11 (MYH11) is a contractile protein belonging to the myosin II superfamily, forming the primary structural component of thick filaments in smooth muscle cells of blood vessels, gastrointestinal tract, and respiratory system. MYH11 consists of an N-terminal globular head domain containing actin-binding and ATPase sites, a neck region that pivots to amplify movement, and an extended α-helical coiled-coil tail domain that dimerizes with another heavy chain and associates with two pairs of regulatory light chains to form the functional hexameric myosin II molecule. MYH11 converts ATP hydrolysis energy into mechanical force by cyclically binding actin, undergoing a power stroke, and dissociating, enabling smooth muscle contraction regulated by RhoA/ROCK/MLC kinase signaling that phosphorylates myosin light chains to relieve inhibition. MYH11 maintains vascular tone, organ motility, and cytoskeletal integrity, interacting with tropomyosin and caldesmon to modulate actin-myosin dynamics during proliferation and migration. Mutations in MYH11 cause familial thoracic aortic aneurysm/dissection by disrupting contractile apparatus stability, while CBFB-MYH11 fusions characterize a favorable-risk acute myeloid leukemia subtype inv(16); additional associations include megacystis-microcolon-intestinal hypoperistalsis syndrome, patent ductus arteriosus, and visceral myopathies.
    References

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