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HSPB8 Protein (AA 1-196) (His tag)

HSPB8 Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant > 95 % by SDS - PAGE SDS
N° du produit ABIN667769
  • Antigène Voir toutes HSPB8 Protéines
    HSPB8 (Heat Shock 22kDa Protein 8 (HSPB8))
    Type de proteíne
    Recombinant
    Attributs du protein
    AA 1-196
    Origine
    • 7
    • 4
    • 3
    • 1
    • 1
    • 1
    Humain
    Source
    • 7
    • 4
    • 3
    • 2
    • 1
    Escherichia coli (E. coli)
    Purification/Conjugué
    Cette HSPB8 protéine est marqué à la His tag.
    Application
    SDS-PAGE (SDS)
    Attributs du produit
    HSPB8/HSP22, 1-196aa, Human, His tag, E.coli
    Pureté
    > 95 % by SDS - PAGE
    Top Product
    Discover our top product HSPB8 Protéine
  • Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/ml (determined by Bradford assay)
    Buffer
    Liquid. In 20mM Tris-HCl buffer (pH 8.0) containing 100mM NaCl, 10% glycerol
    Stock
    4 °C
  • Antigène
    HSPB8 (Heat Shock 22kDa Protein 8 (HSPB8))
    Autre désignation
    HSPB8/HSP22 (HSPB8 Produits)
    Synonymes
    CMT2L Protein, DHMN2 Protein, E2IG1 Protein, H11 Protein, HMN2 Protein, HMN2A Protein, HSP22 Protein, MGC64408 Protein, hsc70 Protein, wu:fb01g06 Protein, wu:fi48b06 Protein, fc09c11 Protein, wu:fc04b04 Protein, wu:fc09c11 Protein, zgc:64202 Protein, AU018630 Protein, AW413033 Protein, Cryac Protein, D5Ucla4 Protein, H11K Protein, HSP20-like Protein, Hsp22 Protein, heat shock protein family B (small) member 8 Protein, heat shock protein family B (small) member 8 L homeolog Protein, heat shock protein 8 Protein, heat shock protein b8 Protein, HSPB8 Protein, hspb8.L Protein, hspa8 Protein, hspb8 Protein, Hspb8 Protein
    Sujet
    Heat shock protein beta-8 (HSPB8), also known as HSP22, member of the small heat shock protein superfamily. HSPB8 is predominantly transcribed in skeletal muscle and heart. The chaperone-like activity is of great importance to the function of HSPB8 in various processes including proliferation, apoptosis and macroautophagy. Mutations in the HSPB8 gene are associated with the inherited peripheral neuropathies, autosomal dominant distal hereditary motor neuropathy type IIA (dSMA) and axonal Charcot-Marie-Tooth disease type 2L (CMT2L). Recombinant human HSPB8, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography techniques. Synonyms: CRYAC, E2IG1, CMT2L, DHMN2, HMN2, HMN2A, Heat shock protein beta-8, heat shock 22kDa protein 8, H11, HSP22, HspB8. NCBI no.: NP_055180
    Poids moléculaire
    23.7 kDa (216aa), confirmed by MALDI-TOF.
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