LETM1 Antikörper (C-Term)

Produktnummer ABIN1537481

Produktdetails anti-LETM1 Antikörper

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

Bindungsspezifität: AA 577-607, C-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser LETM1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

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

Immunogen: 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.

Klon: RB37176

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: LETM1 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Haltbarkeit: 6 months

Details zu LETM1

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

Andere Bezeichnung: LETM1 (LETM1 Produkte)

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

Hintergrund: 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.

Molekulargewicht: 83354

Gen-ID: 3954

NCBI Accession: NP_036450

UniProt: O95202