TSFM antibody (AA 245-346)

Catalog No. ABIN7271022

Product Details anti-TSFM Antibody

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

Binding Specificity: AA 245-346

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TSFM antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Purpose: TSFM Rabbit pAb

Sequence: PSLHKLVLGK YGALVICETS EQKTNLEDVG RRLGQHVVGM APLSVGSLDD EPGGEAETKM LSQPYLLDPS ITLGQYVQPQ GVSVVDFVRF ECGEGEEAAE TE

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 245-346 of human TSFM (NP_001166167).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IF,1:50 - 1:100

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,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.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

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.,TSFM,EFTS,EFTSMT,Epigenetics & Nuclear Signaling,Endocrine & Metabolism,Mitochondrial metabolism,TSFM

Molecular Weight: 18kDa/23kDa/35kDa/37kDa

Gene ID: 10102

UniProt: P43897