GFM1 antibody

Catalog No. ABIN5703276

The Rabbit Polyclonal anti-GFM1 antibody (ABIN5703276) specifically detects GFM1 in WB, IHC, ELISA and IP. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for GFM1 antibody (ABIN5703276)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GFM1 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunoprecipitation (IP)

Product Details anti-GFM1 Antibody

Purpose: GFM1 antibody

Immunogen: G elongation factor, mitochondrial 1

Isotype: IgG

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Comment:

mouse kidney tissue were subjected to SDS PAGE followed by western blot with FNab03430(GFM1 antibody) at dilution of 1:500

Restrictions: For Research Use only

Handling

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: Avoid repeated freeze / thaw cycles.

Storage: -20 °C

Storage Comment: -20°C for 12 months

Expiry Date: 12 months

Target Details for GFM1

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

Alternative Name: GFM1

Background:

Synonyms: Elongation factor G, mitochondrial (EF-Gmt)|Elongation factor G 1, mitochondrial (mEF-G 1)|Elongation factor G1 (hEFG1)|GFM1|EFG|EFG1|GFM

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. Its role in the regulation of normal mitochondrial function and in different disease states attributed to mitochondrial dysfunction is not known.

Molecular Weight: 70 kDa

Gene ID: 85476

UniProt: Q96RP9