ALS2 anticorps (AA 390-470)

N° du produit ABIN7227272

Cet anticorps anti-ALS2 est un anticorps Lapin Polyclonal détectant ALS2 dans WB et ELISA. Adapté pour 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: ALS2 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of ALS2 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 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 (1:500-1:2000), 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 ALS2

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

Autre désignation: ALS2

Sujet: Rabbit Anti-ALS2 Polyclonal Antibody,Alsin, Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 6 protein, Amyotrophic lateral sclerosis 2 protein,ALS2 (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.,ALS2

ID gène: 57679

UniProt: Q96Q42

Pathways: Skeletal Muscle Fiber Development