TSFM antibody (C-Term)

Catalog No. ABIN1536949

Product Details anti-TSFM Antibody

Target: TSFM (Ts Translation Elongation Factor, Mitochondrial (TSFM))

Binding Specificity: AA 253-282, C-Term

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TSFM antibody is un-conjugated

Application: Western Blotting (WB)

Predicted Reactivity: B

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This TSFM antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 253-282 amino acids from the C-terminal region of human TSFM.

Clone: RB35873

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

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: TSFM Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Expiry Date: 6 months

Target Details for TSFM

Target: TSFM (Ts Translation Elongation Factor, Mitochondrial (TSFM))

Alternative Name: TSFM (TSFM Products)

Synonyms: EF-Ts antibody, EF-TsMt antibody, EFTS antibody, zgc:158429 antibody, EFTSMT antibody, 2310050B20Rik antibody, 9430024O13Rik antibody, EF-TS antibody, EF-Tsmt antibody, 2A3-2 antibody, Elongation factor Ts, mitochondrial antibody, Ts translation elongation factor, mitochondrial antibody, Ts translation elongation factor, mitochondrial L homeolog antibody, pco103788 antibody, tsfm antibody, tsfm.L antibody, TSFM antibody, Tsfm antibody

Background: This gene encodes a mitochondrial translation elongation factor. The encoded protein is an enzyme that catalyzes the exchange of guanine nucleotides on the translation elongation factor Tu during the elongation step of mitchondrial protein translation. Mutations in this gene are associated with combined oxidative phosphorylation deficiency-3 syndrome. Alternate splicing results in multiple transcript variants.

Molecular Weight: 35391

Gene ID: 10102

NCBI Accession: NP_001166166, NP_001166167, NP_001166168, NP_005717

UniProt: P43897