TSFM anticorps (C-Term)

N° du produit ABIN1536949

Détail du produit anti-TSFM anticorps

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

Épitope: AA 253-282, C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TSFM est non-conjugé

Application: Western Blotting (WB)

Homologie: B

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

Immunogène: 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

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

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

Date de péremption: 6 months

Détails sur TSFM

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

Autre désignation: TSFM (TSFM Produits)

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

Sujet: 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.

Poids moléculaire: 35391

ID gène: 10102

NCBI Accession: NP_001166166, NP_001166167, NP_001166168, NP_005717

UniProt: P43897