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PMM2 antibody (C-Term)

PMM2 Reactivity: Human WB Host: Rabbit Polyclonal RB39495 unconjugated
Catalog No. ABIN1536830
  • Target See all PMM2 Antibodies
    PMM2 (Phosphomannomutase 2 (PMM2))
    Binding Specificity
    • 9
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 198-226, C-Term
    Reactivity
    • 29
    • 5
    • 5
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    Human
    Host
    • 24
    • 5
    Rabbit
    Clonality
    • 25
    • 3
    Polyclonal
    Conjugate
    • 23
    • 2
    • 1
    • 1
    • 1
    • 1
    This PMM2 antibody is un-conjugated
    Application
    • 28
    • 16
    • 6
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Predicted Reactivity
    B, Pr, M
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    This PMM2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 198-226 amino acids from the C-terminal region of human PMM2.
    Clone
    RB39495
    Isotype
    Ig Fraction
    Top Product
    Discover our top product PMM2 Primary Antibody
  • Application Notes
    WB: 1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    PMM2 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
    Expiry Date
    6 months
  • Target
    PMM2 (Phosphomannomutase 2 (PMM2))
    Alternative Name
    PMM2 (PMM2 Products)
    Background
    The protein encoded by this gene catalyzes the isomerization of mannose 6-phosphate to mannose 1-phosphate, which is a precursor to GDP-mannose necessary for the synthesis of dolichol-P-oligosaccharides. Mutations in this gene have been shown to cause defects in glycoprotein biosynthesis, which manifests as carbohydrate-deficient glycoprotein syndrome type I. [provided by RefSeq].
    Molecular Weight
    28082
    Gene ID
    5373
    NCBI Accession
    NP_000294
    UniProt
    O15305
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