CHRNE anticorps

N° du produit ABIN347199

Cet anticorps anti-CHRNE est un anticorps Lapin Polyclonal détectant CHRNE dans WB, ELISA et IF. Adapté pour Humain et Souris.

Aperçu rapide pour CHRNE anticorps (ABIN347199)

Antigène: CHRNE (Cholinergic Receptor, Nicotinic, epsilon (Muscle) (CHRNE))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CHRNE est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF)

Détail du produit anti-CHRNE anticorps

Specificité: Reacts with human and mouse CHRNE protein

Réactivité croisée: Rat (Rattus)

Réactivité croisée (Details): May cross reacts with protein from rat and other species due to sequence homology (> 80 % ).

Purification: Antiserum

Immunogène: Synthetic peptide derived from the human CHRNE protein.

Isotype: IgG

Information d'application

Indications d'application:

Working dilution: Optimal dilution should be determined by the end user.
The following are guidelines only :
IF(1:200 - 1:1000) WB(1:500 - 1:5000)

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Must be reconstituted in distilled water.

Stock: 4 °C/-20 °C

Stockage commentaire: Lyophilized powder stable for a minimum of 2 years at -20°C. Store reconstituted antibodies at +4°C. For extended periods store in aliquots at -20°C. Antibodies are guaranteed for 6 month from date of receipt.

Date de péremption: 24 months

Détails sur CHRNE

Antigène: CHRNE (Cholinergic Receptor, Nicotinic, epsilon (Muscle) (CHRNE))

Autre désignation: Acetylcholine Receptor Protein, epsilon Subunit (CHRNE)

Sujet: Belongs to the ligand-gated ion channel family. Acetylcholine receptor subfamily. Epsilon/CHRNE sub-subfamily. Defects in CHRNE are a cause of congenital myasthenic syndrome slow-channel type (SCCMS), congenital myasthenic syndrome fast-channel type (FCCMS) and congenital myasthenic syndrome with acetylcholine receptor deficiency (CMS-ACHRD).

ID gène: 1145

UniProt: Q04844