FAHD2A anticorps (AA 121-230) (Biotin)

N° du produit ABIN896020

Cet anticorps Lapin Polyclonal détecte spécifiquement FAHD2A dans WB, ELISA, IHC (p) et IHC (fro). Il présente une réactivité envers Humain.

Aperçu rapide pour FAHD2A anticorps (AA 121-230) (Biotin) (ABIN896020)

Antigène: FAHD2A (Fumarylacetoacetate Hydrolase Domain Containing 2A (FAHD2A))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAHD2A est conjugé à/à la Biotin

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

Détail du produit anti-FAHD2A anticorps (Biotin)

Épitope: AA 121-230

Homologie: Human,Mouse,Rat,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAHD2A

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur FAHD2A

Antigène: FAHD2A (Fumarylacetoacetate Hydrolase Domain Containing 2A (FAHD2A))

Autre désignation: FAHD2A

Sujet:

Synonyms: CGI 105, FAH2A_HUMAN, FAHD 2A, FAHD2A, Fumarylacetoacetate hydrolase domain containing 1, Fumarylacetoacetate hydrolase domain containing 2A, Fumarylacetoacetate hydrolase domain containing protein 2A, Fumarylacetoacetate hydrolase domain-containing protein 2A.

Background: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is also associated with mutations to chromosome 2.

ID gène: 51011