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C10orf2 antibody (C-Term)

C10ORF2 Reactivity: Human WB, IHC (p) Host: Rabbit Polyclonal RB32016 unconjugated
Catalog No. ABIN656726
  • Target See all C10orf2 (C10ORF2) Antibodies
    C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))
    Binding Specificity
    • 7
    • 6
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 656-684, C-Term
    Reactivity
    • 37
    • 14
    • 12
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 36
    • 2
    Rabbit
    Clonality
    • 36
    • 2
    Polyclonal
    Conjugate
    • 16
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    This C10orf2 antibody is un-conjugated
    Application
    • 21
    • 14
    • 12
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    This C10orf2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 656-684 amino acids from the C-terminal region of human C10orf2.
    Clone
    RB32016
    Isotype
    Ig Fraction
    Top Product
    Discover our top product C10ORF2 Primary Antibody
  • Application Notes
    WB: 1:1000. IHC-P: 1:10~50
    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
    C10orf2 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
    Expiry Date
    6 months
  • Target
    C10orf2 (C10ORF2) (Chromosome 10 Open Reading Frame 2 (C10ORF2))
    Alternative Name
    C10orf2 (C10ORF2 Products)
    Background
    This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5' to 3' direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
    Molecular Weight
    77154
    Gene ID
    56652
    NCBI Accession
    NP_001157284, NP_068602
    UniProt
    Q96RR1
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