C6orf168 antibody (AA 221-320) (Cy7)

Catalog No. ABIN1708586

The Rabbit Polyclonal anti-C6orf168 antibody has been validated for WB, IF (cc) and IF (p). It is suitable to detect C6orf168 in samples from Human.

Quick Overview for C6orf168 antibody (AA 221-320) (Cy7) (ABIN1708586)

Target: C6orf168 (FAXC) (Failed Axon Connections Homolog (Drosophila) (FAXC))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C6orf168 antibody is conjugated to Cy7

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

Product Details anti-C6orf168 Antibody (Cy7)

Binding Specificity: AA 221-320

Predicted Reactivity: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C6orf168

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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 C6orf168

Target: C6orf168 (FAXC) (Failed Axon Connections Homolog (Drosophila) (FAXC))

Alternative Name: C6orf168

Background:

Synonyms: C6orf168, CF168_HUMAN, Chromosome 6 open reading frame 168, dJ273F20, Uncharacterized protein C6orf168.

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 C6orf168 gene product has been provisionally designated C6orf168 pending further characterization.

Gene ID: 84553