Fukutin anticorps (C-Term)

N° du produit ABIN2782105

Cet anticorps anti-Fukutin est un anticorps Lapin Polyclonal détectant Fukutin dans WB. Adapté pour Humain, Souris, Rat, Chien, Cheval, Lapin, Cobaye, Boeuf (Vache) et Poisson zèbre (Danio rerio).

Aperçu rapide pour Fukutin anticorps (C-Term) (ABIN2782105)

Antigène: Fukutin (FKTN)

Reactivité: Humain, Souris, Rat, Chien, Cheval, Lapin, Cobaye, Boeuf (Vache), Poisson zèbre (Danio rerio)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Fukutin est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-Fukutin anticorps

Épitope: C-Term

Séquence: FGKVEDSLEL SFQGKDDVKL DVFFFYEETD HMWNGGTQAK TGKKFKYLFP

Homologie: Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 93%, Rabbit: 100%, Rat: 100%, Zebrafish: 86%

Attributs du produit: This is a rabbit polyclonal antibody against FKTN. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the C-terminal region of human FKTN

Information d'application

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: Avoid repeat freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur Fukutin

Antigène: Fukutin (FKTN)

Autre désignation: 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.
Alias Symbols: FCMD, CMD1X, LGMD2M, MDDGA4, MDDGB4, MDDGC4
Protein Size: 329

Poids moléculaire: 36 kDa

ID gène: 2218

NCBI Accession: NM_001079802, NP_001073270

UniProt: O75072

Pathways: Regulation of Carbohydrate Metabolic Process