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GFM2 antibody (AA 436-612)

GFM2 Reactivity: Human IHC, ELISA, WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2686510
$202.21
Plus shipping costs $45.00
100 μL
Shipping to: United States
Delivery in 11 to 21 Business Days
  • Target See all GFM2 Antibodies
    GFM2 (G Elongation Factor, Mitochondrial 2 (GFM2))
    Binding Specificity
    • 15
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 436-612
    Reactivity
    • 32
    • 16
    • 8
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 32
    Rabbit
    Clonality
    • 32
    Polyclonal
    Conjugate
    • 11
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This GFM2 antibody is un-conjugated
    Application
    • 13
    • 13
    • 13
    • 8
    • 5
    • 4
    • 3
    • 2
    • 2
    Immunohistochemistry (IHC), ELISA, Western Blotting (WB)
    Purification
    Affinity purified
    Immunogen
    Rabbit polyclonal GFM2(1) antibody was raised against a recombinate human GFM2 protein 436-612 aa (BC015712).
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    PBS, pH 7.4 with 0.02 % 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
  • Target
    GFM2 (G Elongation Factor, Mitochondrial 2 (GFM2))
    Alternative Name
    GFM2 (GFM2 Products)
    Synonyms
    RGD1309854, 6530419G12Rik, A930009M04Rik, EF-G2mt, EFG2, MST027, RRF2mt, mEF-G 2, si:dkey-35i22.3, zgc:153835, MRRF2, RRF2, hEFG2, ST15, G elongation factor, mitochondrial 2, G elongation factor mitochondrial 2, ribosome-releasing factor 2, mitochondrial, reversion inducing cysteine rich protein with kazal motifs, Gfm2, GFM2, gfm2, LOC662021, RECK
    Background
    Eukaryotes contain two protein translational systems, one in the cytoplasm and one in the mitochondria. Mitochondrial translation is crucial for maintaining mitochondrial function and mutations in this system lead to a breakdown in the respiratory chain-oxidative phosphorylation system and to impaired maintenance of mitochondrial DNA. This gene encodes one of the mitochondrial translation elongation factors, which is a GTPase that plays a role at the termination of mitochondrial translation by mediating the disassembly of ribosomes from messenger RNA . Its role in the regulation of normal mitochondrial function and in disease states attributed to mitochondrial dysfunction is not known. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2013]
    Pathways
    Ribonucleoprotein Complex Subunit Organization
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