C6orf192 antibody (AA 50-80) (FITC)

Catalog No. ABIN1403258

Product Details anti-C6orf192 Antibody (FITC)

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

Binding Specificity: AA 50-80

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C6orf192 antibody is conjugated to FITC

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

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C6orf192

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for C6orf192

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

Alternative Name: C6orf192 (C6orf192 Products)

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

Background:

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.

Gene ID: 116843

UniProt: Q6NT16