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HSPB8 antibody

HSPB8 Reactivity: Human, Mouse, Rat WB, EIA, IHC (fro) Host: Mouse Monoclonal 3C12-H11 unconjugated
Catalog No. ABIN492450
  • Target See all HSPB8 Antibodies
    HSPB8 (Heat Shock 22kDa Protein 8 (HSPB8))
    Reactivity
    • 86
    • 34
    • 21
    • 4
    • 4
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 63
    • 22
    • 1
    Mouse
    Clonality
    • 58
    • 28
    Monoclonal
    Conjugate
    • 39
    • 7
    • 6
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This HSPB8 antibody is un-conjugated
    Application
    • 70
    • 35
    • 27
    • 26
    • 25
    • 14
    • 13
    • 12
    • 10
    • 5
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Enzyme Immunoassay (EIA), Immunohistochemistry (Frozen Sections) (IHC (fro))
    Specificity
    Detects endogenous and exogenous hsp22 in monomeric, dimeric and tetrameric (weak) forms in Western Blot. Does not cross react with alpha Crystalline. Exogenous HSP22 detected in dimeric form.
    Characteristics
    Synonyms: Alpha crystallin C chain, CMT2L, CRYAC, DHMN2, H11, Heat shock 22kDa protein 8, HMN2,HSB8, HspB8
    Purification
    Protein G Chromatography.
    Immunogen
    His-tagged Human recombinant HSP22
    Clone
    3C12-H11
    Isotype
    IgG1
    Top Product
    Discover our top product HSPB8 Primary Antibody
  • Application Notes
    ELISA. Western blot (1/2000).1 μg/mL was sufficient for detection of Hsp22 in 20 μg of whole rat tissue extract by ECLimmunoblot analysis using Goat anti-mouse IgG: HRP as the secondary antibody. Immunohistochemistry.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.
    Restrictions
    For Research Use only
  • Concentration
    1.0 mg/mL
    Buffer
    PBS, pH 7.4 containing 50 % Glycerol as stabilizer and 0.09 % Sodium Azide as preservative.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer. Avoid repeated freezing and thawing.
    Shelf life: one year from despatch.
    Expiry Date
    12 months
  • Target
    HSPB8 (Heat Shock 22kDa Protein 8 (HSPB8))
    Alternative Name
    HSP22 (HSPB8 Products)
    Synonyms
    CMT2L antibody, DHMN2 antibody, E2IG1 antibody, H11 antibody, HMN2 antibody, HMN2A antibody, HSP22 antibody, MGC64408 antibody, hsc70 antibody, wu:fb01g06 antibody, wu:fi48b06 antibody, fc09c11 antibody, wu:fc04b04 antibody, wu:fc09c11 antibody, zgc:64202 antibody, AU018630 antibody, AW413033 antibody, Cryac antibody, D5Ucla4 antibody, H11K antibody, HSP20-like antibody, Hsp22 antibody, heat shock protein family B (small) member 8 antibody, heat shock protein family B (small) member 8 L homeolog antibody, heat shock protein 8 antibody, heat shock protein b8 antibody, HSPB8 antibody, hspb8.L antibody, hspa8 antibody, hspb8 antibody, Hspb8 antibody
    Background
    Hsp22 (HSPB8) is a 196-amino acid protein that is a member of the small heat shock protein super-family and the human protein is most closely related to Hsp27. Similar to most other sHSPs, Hsp22 is predominately transcribed in skeletal muscle and heart, as well as the placenta (1). Hsp22 is a monomeric protein which interacts with HSPB1. It displays temperature-dependent chaperone activity. In a two hybrid screen, HspB8 interacted preferentially with a triple aspartate form of Hsp27 which mimics Hsp27 phosphorylated at Ser15, Ser78, and Ser82, as compared to wild-type Hsp27 (2). HSPB8 has two binding domains (N and C Terminal) that are specific for different binding partners, and has the ability to bind itself and other sHSPs (3). The chaperone-like activity is of great importance to the function of Hsp22 in various processes including proliferation, apoptosis and macroautophagy (4). Mutations in the HSPB8 gene are associated with the inherited peripheral neurpathies, autosomal dominant distal hereditary motor neuropathy type IIA (dSMA) and axonal Charcot-Marie-Tooth disease type 2L (CMT2L) (5).Synonyms: Alpha crystallin C chain, CMT2L, CRYAC, DHMN2, H11, HMN2, HSB8, Heat shock 22 kDa protein 8, HspB8
    Gene ID
    2030
    UniProt
    Q9UJY2
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