HGD anticorps (AA 374-445)

N° du produit ABIN7998311

Cet anticorps anti-HGD Monoclonal Souris (Clone 2F11E1) (ABIN7998311) détecte spécifiquement HGD dans WB, IHC et FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour HGD anticorps (AA 374-445) (ABIN7998311)

Antigène: HGD (Homogentisate 1,2-Dioxygenase (HGD))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp HGD est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)

Classe de qualité: Carrier-free

Clone: 2F11E1

Détail du produit anti-HGD anticorps

Épitope: AA 374-445

Fonction: Anti-HGD Antibody (monoclonal, 2F11E1)

Réactivité croisée (Details): No cross-reactivity with other proteins.

Attributs du produit: Anti-HGD Antibody.(monoclonal, 2F11E1)-1. Tested in Flow Cytometry, IHC, WB applications. This antibody reacts with Human.

Purification: Immunogen affinity purified.

Immunogène: E. coli-derived human HGD recombinant protein (Position: D374-N445).

Isotype: IgG2b

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Human Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur HGD

Antigène: HGD (Homogentisate 1,2-Dioxygenase (HGD))

Autre désignation: HGD

Sujet:

Background: The HGD gene encodes homogentisate 1,2-dioxygenase (HGD), an enzyme involved in the catabolism of phenylalanine and tyrosine. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria. This gene is mapped to chromosome 3q21-q23 by a preliminary PCR screen of hamster/human somatic cell hybrid genomic DNA samples and by fluorescence in situ hybridization.

Gene Full Name: homogentisate 1,2-dioxygenase

Poids moléculaire: 50 kDa

ID gène: 3081

UniProt: Q93099