LETM1 anticorps (C-Term)

N° du produit ABIN1537481

Détail du produit anti-LETM1 anticorps

Antigène: LETM1 (Leucine Zipper-EF-Hand Containing Transmembrane Protein 1 (LETM1))

Épitope: AA 577-607, C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LETM1 est non-conjugé

Application: Western Blotting (WB)

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

Immunogène: This LETM1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 577-607 amino acids from the C-terminal region of human LETM1.

Clone: RB37176

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: LETM1 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 LETM1

Antigène: LETM1 (Leucine Zipper-EF-Hand Containing Transmembrane Protein 1 (LETM1))

Autre désignation: LETM1 (LETM1 Produits)

Synonymes: anticorps LETM1, anticorps wu:fc31h08, anticorps wu:fc58h01, anticorps zgc:109969, anticorps letm1, anticorps MGC145623, anticorps leucine zipper and EF-hand containing transmembrane protein 1, anticorps leucine zipper-EF-hand containing transmembrane protein 1, anticorps LETM1 and EF-hand domain-containing protein 1, mitochondrial, anticorps LETM1, anticorps letm1, anticorps LOC100346816, anticorps Letm1

Sujet: This gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.

Poids moléculaire: 83354

ID gène: 3954

NCBI Accession: NP_036450

UniProt: O95202