Leucine Zipper And EF-Hand Containing Transmembrane Protein 1 (LETM1) Antibody

Product Graph
169€ (20 µg)

Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.

935106861
info@markelab.com
name
Leucine Zipper And EF-Hand Containing Transmembrane Protein 1 (LETM1) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx338717
tested applications
ELISA, WB, IHC, IF/ICC

Description

LETM1 Antibody is a Rabbit Polyclonal against LETM1.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Leucine Zipper And EF-Hand Containing Transmembrane Protein 1 (LETM1)
Host
Rabbit
Reactivity
Human, Mouse
Recommended Dilution
WB: 1/500 - 1/5000, IHC: 1/200 - 1/500, IF/ICC: 1/50 - 1/200. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purity
> 95%
Purification
Purified by Protein G.
Size 1
20 µg
Size 2
50 µg
Size 3
100 µg
Size 4
200 µg
Size 5
1 mg
Form
Liquid
Tested Applications
ELISA, WB, IHC, IF/ICC
Buffer
0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% Glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
O95202
Gene ID
3954
Background
Antibody anti-LETM1
Status
RUO

Descripción

Related Products

FNab04755

LETM1 antibody

Crucial for the maintenance of mitochondrial tubular networks and for the assembly of the supercomplexes of the respiratory chain. Required for the maintenance of the tubular shape and cristae organization.

Ver Producto
P8567

Recombinant Human LETM1

Ver Producto
abx029535

Leucine Zipper And EF-Hand Containing Transmembrane Protein 1 (LETM1) Antibody

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.

Ver Producto