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COG8 antibody (N-Term)

COG8 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5517541
  • Target See all COG8 Antibodies
    COG8 (Component of Oligomeric Golgi Complex 8 (COG8))
    Binding Specificity
    • 4
    • 2
    • 1
    N-Term
    Reactivity
    • 9
    • 1
    • 1
    Human
    Host
    • 6
    • 2
    • 1
    Rabbit
    Clonality
    • 9
    Polyclonal
    Conjugate
    • 6
    • 1
    • 1
    • 1
    This COG8 antibody is un-conjugated
    Application
    • 5
    • 4
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Sequence
    MATAATIPSV ATATAAALGE VEDEGLLASL FRDRFPEAQW RERPDVGRYL
    Purification
    Affinity purified
    Immunogen
    The immunogen is a synthetic peptide directed towards the N terminal region of human COG8
    Top Product
    Discover our top product COG8 Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    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
    -20 °C
    Storage Comment
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target
    COG8 (Component of Oligomeric Golgi Complex 8 (COG8))
    Alternative Name
    COG8 (COG8 Products)
    Synonyms
    CDG2H antibody, DOR1 antibody, BB235941 antibody, C87832 antibody, component of oligomeric golgi complex 8 antibody, Cog8 antibody, cog8 antibody, COG8 antibody
    Background
    This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance.

    Alias Symbols: DOR1, CDG2H

    Protein Size: 612
    Gene ID
    84342
    NCBI Accession
    NM_032382, NP_115758
    UniProt
    Q96MW5
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