AFG3L2 anticorps (N-Term)

N° du produit ABIN7467943

L’anticorps Lapin Polyclonal anti-AFG3L2 a été validé pour WB et IHC (p). Il convient pour détecter AFG3L2 dans des échantillons de Humain.

Aperçu rapide pour AFG3L2 anticorps (N-Term) (ABIN7467943)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AFG3L2 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-AFG3L2 anticorps

Épitope: N-Term

Réactivité croisée: Humain, Rat

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the N-terminus region of human AFG3L2. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: SK-N-SH membrane fraction extract Validation: Orthogonal

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur AFG3L2

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

Autre désignation: AFG3 like matrix AAA peptidase subunit 2

Sujet:

Synonyms: AFG3 like matrix AAA peptidase subunit 2 , SCA28 , SPAX5

Background: This gene 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. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq]

Poids moléculaire: 89 kDa

ID gène: 10939

UniProt: Q9Y4W6

Pathways: Skeletal Muscle Fiber Development