Fukutin anticorps (AA 177-206)

N° du produit ABIN5534447

Détail du produit anti-Fukutin anticorps

Antigène: Fukutin (FKTN)

Épitope: AA 177-206

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Fukutin est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

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

Immunogène: This FKTN antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 177-206 amino acids from the Central region of human FKTN.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

For IHC-P starting dilution is: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: 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: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur Fukutin

Antigène: Fukutin (FKTN)

Autre désignation: FKTN (FKTN Produits)

Synonymes: anticorps FCMD, anticorps fcmd, anticorps im:7163166, anticorps zgc:162828, anticorps FKTN, anticorps CMD1X, anticorps LGMD2M, anticorps MDDGA4, anticorps MDDGB4, anticorps MDDGC4, anticorps D830030O17Rik, anticorps Fcmd, anticorps fukutin, anticorps fukutin S homeolog, anticorps Fukutin, anticorps FKTN, anticorps fktn, anticorps fktn.S, anticorps Bm1_09375, anticorps Bm1_09380, anticorps Bm1_44655, anticorps Fktn

Sujet: The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene.

Poids moléculaire: 54 kDa

ID gène: 2218

UniProt: O75072

Pathways: Regulation of Carbohydrate Metabolic Process