Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

POMT1 antibody

POMT1 Reactivity: Human WB, IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2433621
  • Target See all POMT1 Antibodies
    POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))
    Reactivity
    • 43
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 44
    Rabbit
    Clonality
    • 44
    Polyclonal
    Conjugate
    • 18
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This POMT1 antibody is un-conjugated
    Application
    • 29
    • 19
    • 17
    • 16
    • 13
    • 13
    • 7
    • 3
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human POMT1
    Isotype
    IgG
    Top Product
    Discover our top product POMT1 Primary Antibody
  • Application Notes
    WB 1:500-1:2000, IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.9 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Handling Advice
    Avoid freeze / thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))
    Alternative Name
    POMT1 (POMT1 Products)
    Synonyms
    LGMD2K antibody, MDDGA1 antibody, MDDGB1 antibody, MDDGC1 antibody, RT antibody, AI505244 antibody, protein O-mannosyltransferase 1 antibody, protein-O-mannosyltransferase 1 antibody, POMT1 antibody, Pomt1 antibody
    Background
    The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.
    Molecular Weight
    Calculated MW: 85 kDa
    NCBI Accession
    NP_009102
You are here:
Support