CHM antibody

Product Graph
Contáctenos para saber el precio

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

935106861
info@markelab.com
name
CHM antibody
category
Primary Antibodies
provider
FineTest
reference
FNab10380
tested applications
ELISA, WB, IHC

Documents del producto

Instrucciones
Descargar
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Rab proteins geranylgeranyltransferase component A 1 (CHM)
Host
Rabbit
Reactivity
Human
Recommended Dilution
WB: 1:500-1:2000; IHC: 1:20-1:200
Clonality
polyclonal
Conjugation
Unconjugated
Isotype
IgG
Observed MW
100 kDa, 60 kDa
Purity
≥95% as determined by SDS-PAGE
Purification
Immunogen affinity purified
Size 1
100µg
Form
liquid
Tested Applications
ELISA, WB, IHC
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.)
UniProt ID
P24386
Alias
Rab proteins geranylgeranyltransferase component A 1,Choroideremia protein,Rab escort protein 1 (REP-1),TCD protein,CHM,REP1,TCD
Background
Antibody anti-CHM
Status
RUO
Note
Mol. Weight 100 kDa, 60 kDa

Related Products

FNab10380

CHM antibody

Ver Producto
abx005801

Rab Proteins Geranylgeranyltransferase Component A 1 (CHM) Antibody

CHM Antibody is a Rabbit Polyclonal Antibody against CHM.

Ver Producto
abx031377

Rab Proteins Geranylgeranyltransferase Component A 1 (CHM) Antibody

This gene encodes component A of the RAB geranylgeranyl transferase holoenzyme. In the dimeric holoenzyme, this subunit binds unprenylated Rab GTPases and then presents them to the catalytic Rab GGTase subunit for the geranylgeranyl transfer reaction. Rab GTPases need to be geranylgeranyled on either one or two cysteine residues in their C-terminus to localize to the correct intracellular membrane. Mutations in this gene are a cause of choroideremia; also known as tapetochoroidal dystrophy (TCD). This X-linked disease is characterized by progressive dystrophy of the choroid, retinal pigment epithelium and retina. Alternative splicing results in multiple transcript variants encoding different isoforms.

Ver Producto