ALS2 anticorps (AA 390-470)

N° du produit ABIN7227272

Cet anticorps anti-ALS2 Polyclonal Lapin (ABIN7227272) détecte spécifiquement ALS2 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour ALS2 anticorps (AA 390-470) (ABIN7227272)

Antigène: ALS2 (Amyotrophic Lateral Sclerosis 2 (Juvenile) (ALS2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALS2 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-ALS2 anticorps

Épitope: AA 390-470

Fonction: Rabbit Anti-ALS2 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of ALS2 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 ALS2 protein at AA range: 390-470

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 ALS2

Antigène: ALS2 (Amyotrophic Lateral Sclerosis 2 (Juvenile) (ALS2))

Autre désignation: ALS2

Sujet: Alsin, Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 6 protein, Amyotrophic lateral sclerosis 2 proteinALS2 (ALS2, Alsin Rho Guanine Nucleotide Exchange Factor) is a Protein Coding gene. Diseases associated with ALS2 include Primary Lateral Sclerosis, Juvenile and Spastic Paralysis, Infantile Onset Ascending. Among its related pathways are RAB GEFs exchange GTP for GDP on RABs and Vesicle-mediated transport.

Poids moléculaire: 182kD

ID gène: 57679

UniProt: Q96Q42

Pathways: Skeletal Muscle Fiber Development