Chromosome 6 Open Reading Frame 134 (C6orf134) (AA 30-80) anticorps (Biotin)

N° du produit ABIN1403287

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

Aperçu rapide pour Chromosome 6 Open Reading Frame 134 (C6orf134) (AA 30-80) anticorps (Biotin) (ABIN1403287)

Antigène: Chromosome 6 Open Reading Frame 134 (C6orf134)

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Biotin

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

Détail du produit

Épitope: AA 30-80

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human alpha-TAT

Isotype: IgG

Information d'application

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

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

Détail du antigène

Antigène: Chromosome 6 Open Reading Frame 134 (C6orf134)

Autre désignation: alpha-TAT

Sujet:

Synonyms: C6orf134, Acetyltransferase mec 17 homolog, Alpha TAT, Alpha tubulin acetyltransferase 1, Alpha tubulin N acetyltransferase, Chromosome 6 open reading frame 134, Hypothetical protein LOC79969, MEC17, Nbla00487, TAT, ATAT_HUMAN.

Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf134 gene product has been provisionally designated C6orf134 pending further characterization.

ID gène: 79969

UniProt: Q5SQI0