C6ORF195 anticorps (AA 81-127) (Biotin)

N° du produit ABIN1699923

Détail du produit anti-C6ORF195 anticorps (Biotin)

Antigène: C6ORF195 (Chromosome 6 Open Reading Frame 195 (C6ORF195))

Épitope: AA 81-127

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C6ORF195 est conjugé à/à la Biotin

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

Homologie: Human

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C6orf195

Isotype: IgG

Information d'application

Indications d'application: 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 C6ORF195

Antigène: C6ORF195 (Chromosome 6 Open Reading Frame 195 (C6ORF195))

Autre désignation: C6orf195 (C6ORF195 Produits)

Synonymes: anticorps RP11-145H9.2, anticorps bA145H9.2, anticorps long intergenic non-protein coding RNA 1600, anticorps LINC01600

Sujet:

Synonyms: bA145H9.2, C6orf195, CF195_HUMAN, Chromosome 6 open reading frame 195, FLJ31934, RP11-145H9.2, Uncharacterized protein C6orf195.

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 C6orf195 gene product has been provisionally designated C6orf195 pending further characterization.

ID gène: 154386