C6ORF62 anticorps (Alexa Fluor 647)

N° du produit ABIN1403076

Détail du produit anti-C6ORF62 anticorps (Alexa Fluor 647)

Antigène: C6ORF62 (Chromosome 6 Open Reading Frame 62 (C6ORF62))

Reactivité: Souris, Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C6ORF62 est conjugé à/à la Alexa Fluor 647

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C6orf62

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur C6ORF62

Antigène: C6ORF62 (Chromosome 6 Open Reading Frame 62 (C6ORF62))

Autre désignation: C6orf62 (C6ORF62 Produits)

Synonymes: anticorps Nbla00237, anticorps XTP12, anticorps dJ30M3.2, anticorps C6orf62, anticorps 8030460C05Rik, anticorps C78201, anticorps chromosome 6 open reading frame 62, anticorps chromosome 2 open reading frame, human C6orf62, anticorps cDNA sequence BC005537, anticorps chromosome 6 open reading frame, human C6orf62, anticorps chromosome 23 open reading frame, human C6orf62, anticorps C6orf62, anticorps C2H6ORF62, anticorps BC005537, anticorps C6H6orf62, anticorps C23H6orf62

Sujet:

Synonyms: C6orf62, CF062_HUMAN, HBV X-transactivated gene 12 protein, HBV XAg-transactivated protein 12, Nbla00237, Uncharacterized protein C6orf62, XTP12.

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 C6orf62 gene product has been provisionally designated C6orf62 pending further characterization.

ID gène: 81688