AMPD3 anticorps

N° du produit ABIN6251794

L’anticorps Souris Monoclonal anti-AMPD3 a été validé pour IF, ICC et IHC (p). Il convient pour détecter AMPD3 dans des échantillons de Humain.

Aperçu rapide pour AMPD3 anticorps (ABIN6251794)

Antigène: AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp AMPD3 est non-conjugé

Application: Immunofluorescence (IF), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: ETAD3-1

Détail du produit anti-AMPD3 anticorps

Purification: Protein G affinity chromatography

Immunogène: Recombinant full-length human protein was used as the immunogen for the AMPD3 antibody.

Isotype: IgG2b kappa

Information d'application

Indications d'application: Immunofluorescence: 0.5-1 μg/mL

Immunocytochemistry: 1-2 μg/mL for 30 min at RT

Immunohistology (FFPE): 2-4 μg/mL for 30 min at RT (1)

Prediluted format : incubate for 30 min at RT (2)

Optimal dilution of the AMPD3 antibody should be determined by the researcher.

1. Staining of formalin-fixed tissues requires boiling tissue sections in 10  mM Citrate buffer,  pH 6.0, for 10-20 min followed by cooling at RT for 20 min
2. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.2 mg/mL

Buffer: PBS with 0.1 mg/mL BSA and 0.05 % sodium azide

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: Aliquot and Store at -20C. Avoid freez-thaw cycles.

Détails sur AMPD3

Antigène: AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))

Autre désignation: AMPD3

Sujet: AMPD3 is a member of the AMP deaminase gene family. It is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in the gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. [RefSeq]

ID gène: 272

UniProt: Q01432