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Transmembrane Protein 70 (TMM70) (AA 231-260), (C-Term) antibody

TMM70 Reactivity: Human WB, IHC (p) Host: Rabbit Polyclonal RB32747 unconjugated
Catalog No. ABIN2846127
  • Target See all Transmembrane Protein 70 (TMM70) Antibodies
    Transmembrane Protein 70 (TMM70)
    Binding Specificity
    • 8
    • 8
    • 7
    • 1
    • 1
    • 1
    AA 231-260, C-Term
    Reactivity
    • 19
    • 3
    • 2
    Human
    Host
    • 18
    • 1
    Rabbit
    Clonality
    • 18
    • 1
    Polyclonal
    Conjugate
    • 9
    • 2
    • 2
    • 2
    • 2
    • 2
    Un-conjugated
    Application
    • 19
    • 14
    • 14
    • 5
    • 2
    • 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 TMM70 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 231-260 amino acids from the C-terminal region of human TMM70.
    Clone
    RB32747
    Isotype
    Ig Fraction
  • 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
    TMM70 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
    Transmembrane Protein 70 (TMM70)
    Alternative Name
    TMM70 (TMM70 Products)
    Synonyms
    MC5DN2 antibody, 1110020A09Rik antibody, 2210416J16Rik antibody, RGD1566224 antibody, transmembrane protein 70 antibody, TMEM70 antibody, Tmem70 antibody
    Background
    This gene likely encodes a mitochondrial membrane protein. The encoded protein may play a role in biogenesis of mitochondrial ATP synthase. Mutations in this gene have been associated with neonatal mitochondrial encephalocardiomyopathy due to ATP synthase deficiency. Alternatively spliced transcript variants have been described.
    Molecular Weight
    28969
    Gene ID
    54968
    NCBI Accession
    NP_001035703, NP_060336
    UniProt
    Q9BUB7
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