CLCN1 anticorps

N° du produit ABIN7227934

L’anticorps Lapin Polyclonal anti-CLCN1 a été validé pour WB et ELISA. Il convient pour détecter CLCN1 dans des échantillons de Humain.

Aperçu rapide pour CLCN1 anticorps (ABIN7227934)

Antigène: CLCN1 (Chloride Channel 1, Skeletal Muscle (CLCN1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CLCN1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-CLCN1 anticorps

Fonction: CLCN1 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of CLCN1 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 CLCN1 protein

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 CLCN1

Antigène: CLCN1 (Chloride Channel 1, Skeletal Muscle (CLCN1))

Autre désignation: CLCN1

Sujet: Rabbit Anti-CLCN1 Polyclonal Antibody,Chloride channel protein 1, ClC-1, Chloride channel protein, skeletal muscle,CLCN1 (Chloride Voltage-Gated Channel 1) is a Protein Coding gene. Diseases associated with CLCN1 include Myotonia Congenita, Recessive and Myotonia Congenita, Dominant The protein encoded by CLCN1 regulates the electric excitability of the skeletal muscle membrane. Mutations in CLCN1 cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen). Alternative splicing results in multiple transcript variants.,CLCN1

Poids moléculaire: observerd band 108kDa

ID gène: 1180

UniProt: P35523