C6orf192 anticorps (AA 50-80) (Alexa Fluor 350)

N° du produit ABIN1403253

Détail du produit anti-C6orf192 anticorps (Alexa Fluor 350)

Antigène: C6orf192 (Chromosome 6 Open Reading Frame 192 (C6orf192))

Épitope: AA 50-80

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C6orf192 est conjugé à/à la Alexa Fluor 350

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 C6orf192

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 C6orf192

Antigène: C6orf192 (Chromosome 6 Open Reading Frame 192 (C6orf192))

Autre désignation: C6orf192 (C6orf192 Produits)

Synonymes: anticorps C3H6orf192, anticorps SLC18B1, anticorps C6orf192, anticorps dJ55C23.6, anticorps 1110021L09Rik, anticorps solute carrier family 18, subfamily B, member 1, anticorps solute carrier family 18 member B1, anticorps slc18b1, anticorps SLC18B1, anticorps Slc18b1

Sujet:

Synonyms: C6orf192, dJ55C23.6, MFS-type transporter SLC18B1, Solute carrier family 18 member B1, SLC18B1

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 C6orf192 gene product has been provisionally designated C6orf192 pending further characterization.

ID gène: 116843

UniProt: Q6NT16