C8orf47 anticorps (AA 1-100) (Biotin)

N° du produit ABIN1699940

L’anticorps Lapin Polyclonal anti-C8orf47 a été validé pour WB. Il convient pour détecter C8orf47 dans des échantillons de Humain.

Aperçu rapide pour C8orf47 anticorps (AA 1-100) (Biotin) (ABIN1699940)

Antigène: C8orf47 (C8ORF47) (Chromosome 8 Open Reading Frame 47 (C8ORF47))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C8orf47 est conjugé à/à la Biotin

Application: Western Blotting (WB)

Détail du produit anti-C8orf47 anticorps (Biotin)

Épitope: AA 1-100

Réactivité croisée: Humain

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C8orf47

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000

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 C8orf47

Antigène: C8orf47 (C8ORF47) (Chromosome 8 Open Reading Frame 47 (C8ORF47))

Autre désignation: C8orf47

Sujet:

Synonyms: C8orf47, CH047_HUMAN, Chromosome 8 open reading frame 47, Uncharacterized protein C8orf47.

Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf47 gene product has been provisionally designated C8orf47 pending further characterization.

ID gène: 203111