CLCN1 anticorps

N° du produit ABIN7227934

L’anticorps anti-CLCN1 Polyclonal Lapin est utilisé pour la détection de CLCN1 dans des échantillons de Humain, Souris et Rat. Il a été validé pour WB et ELISA.

Aperçu rapide pour CLCN1 anticorps (ABIN7227934)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CLCN1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-CLCN1 anticorps

Fonction: Rabbit Anti-CLCN1 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of CLCN1 protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-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 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: 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.

Date de péremption: 12 months

Détails sur CLCN1

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

Autre désignation: CLCN1

Sujet: Chloride channel protein 1, ClC-1, Chloride channel protein, skeletal muscleCLCN1 (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.

Poids moléculaire: 108kD

ID gène: 1180

UniProt: P35523