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GFM1 antibody

This Rabbit Polyclonal antibody specifically detects GFM1 in WB and ELISA. It exhibits reactivity toward Human.
Catalog No. ABIN7228362

Quick Overview for GFM1 antibody (ABIN7228362)

Target

See all GFM1 Antibodies
GFM1 (G-Elongation Factor, Mitochondrial 1 (GFM1))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This GFM1 antibody is un-conjugated

Application

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Western Blotting (WB), ELISA
  • Purpose

    EFGM Polyclonal Antibody

    Specificity

    The antibody detects endogenous levels of EFGM protein

    Purification

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    Immunogen

    Synthesized peptide derived from part region of human EFGM protein

    Isotype

    IgG
  • Application Notes

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    Comment

    Primary Antibody

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • Target

    GFM1 (G-Elongation Factor, Mitochondrial 1 (GFM1))

    Alternative Name

    EFGM

    Background

    Rabbit Anti-EFGM Polyclonal Antibody,Elongation factor G, mitochondrial, EF-Gmt, Elongation factor G 1, mitochondrial, mEF-G 1, Elongation factor G1, hEFG1,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. Its role in the regulation of normal mitochondrial function and in different disease states attributed to mitochondrial dysfunction is not known.,EFGM

    Molecular Weight

    observerd band 82kDa

    Gene ID

    85476

    UniProt

    Q96RP9
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