FAM78A anticorps (Biotin)

N° du produit ABIN1403905

Détail du produit anti-FAM78A anticorps (Biotin)

Antigène: FAM78A (Family with Sequence Similarity 78, Member A (FAM78A))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM78A est conjugé à/à la Biotin

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

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAM78A/C9orf59

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

Détails sur FAM78A

Antigène: FAM78A (Family with Sequence Similarity 78, Member A (FAM78A))

Autre désignation: C9orf59 (FAM78A Produits)

Synonymes: anticorps fam78a, anticorps zgc:175187, anticorps C9orf59, anticorps A130092J06Rik, anticorps RGD1566351, anticorps family with sequence similarity 78 member A, anticorps family with sequence similarity 78, member Ab, anticorps family with sequence similarity 78, member A, anticorps FAM78A, anticorps fam78ab, anticorps fam78a, anticorps Fam78a

Sujet:

Synonyms: C9orf59, Chromosome 9 open reading frame 59, Family with sequence similarity 78, member A, FLJ00024, Hypothetical protein LOC286336,FAM78A.

Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The FAM78A gene product has been provisionally designated FAM78A pending further characterization.

ID gène: 286336