Fukutin anticorps (AA 111-160)

N° du produit ABIN7228550

Cet anticorps Lapin Polyclonal détecte spécifiquement Fukutin dans WB et ELISA. Il présente une réactivité envers Humain et Souris.

Aperçu rapide pour Fukutin anticorps (AA 111-160) (ABIN7228550)

Antigène: Fukutin (FKTN)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Fukutin est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Fukutin anticorps

Épitope: AA 111-160

Fonction: FKTN Polyclonal Antibody

Specificité: The antibody detects endogenous levels of FKTN protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogène: Synthesized peptide derived from part region of human FKTN protein at AA range: 111-160

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Détails sur Fukutin

Antigène: Fukutin (FKTN)

Autre désignation: FKTN

Sujet: Rabbit Anti-FKTN Polyclonal Antibody,Fukutin, Fukuyama-type congenital muscular dystrophy protein,The protein encoded by FKTN 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 FKTN 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 FKTN.,FKTN

Poids moléculaire: observerd band 50kDa

ID gène: 2218

UniProt: O75072

Pathways: Regulation of Carbohydrate Metabolic Process