AFG3L2 anticorps (AA 744-793)

N° du produit ABIN7227232

Cet anticorps anti-AFG3L2 est un anticorps Lapin Polyclonal détectant AFG3L2 dans WB et ELISA. Adapté pour Humain.

Aperçu rapide pour AFG3L2 anticorps (AA 744-793) (ABIN7227232)

Antigène: AFG3L2 (AFG3-Like Protein 2 (AFG3L2))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AFG3L2 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-AFG3L2 anticorps

Épitope: AA 744-793

Fonction: AFG3L2 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of AFG3L2

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogène: Synthesized peptide derived from part region of human AFG3L2 protein at AA range: 744-793

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 (1:10000-1:20000).

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 as stabilizer.

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 AFG3L2

Antigène: AFG3L2 (AFG3-Like Protein 2 (AFG3L2))

Autre désignation: AFG3L2

Sujet: Rabbit Anti-AFG3L2 Polyclonal Antibody,AFG3-like protein 2, Paraplegin-like protein,AFG3L2 (AFG3 Like Matrix AAA Peptidase Subunit 2) is a Protein Coding gene. Diseases associated with AFG3L2 include Spinocerebellar Ataxia 28 and Spastic Ataxia 5, Autosomal Recessive. AFG3L2 encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. AFG3L2 is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.,AFG3L2

ID gène: 10939

UniProt: Q9Y4W6

Pathways: Skeletal Muscle Fiber Development