FAHD1 anticorps (AA 101-200) (Biotin)

N° du produit ABIN1700655

Cet anticorps anti-FAHD1 est un anticorps Lapin Polyclonal détectant FAHD1 dans WB, ELISA, IHC (fro) et IHC (p). Adapté pour Humain.

Aperçu rapide pour FAHD1 anticorps (AA 101-200) (Biotin) (ABIN1700655)

Antigène: FAHD1 (Fumarylacetoacetate Hydrolase Domain Containing 1 (FAHD1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAHD1 est conjugé à/à la Biotin

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

Détail du produit anti-FAHD1 anticorps (Biotin)

Épitope: AA 101-200

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAHD1

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 FAHD1

Antigène: FAHD1 (Fumarylacetoacetate Hydrolase Domain Containing 1 (FAHD1))

Autre désignation: FAHD1

Sujet:

Synonyms: Acylpyruvase FAHD1, C16orf36, Chromosome 16 open reading frame 36, DKFZP566J2046, FAHD1, FAHD1_HUMAN, Fumarylacetoacetate hydrolase domain containing protein 1, Fumarylacetoacetate hydrolase domain-containing protein 1, MGC74876, mitochondrial, YISK like, YISK like/RJD15, YisK-like protein, YISKL.

Background: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3 % of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

ID gène: 81889