C12ORF29 antibody (Alexa Fluor 350)

Catalog No. ABIN1405599

Product Details anti-C12ORF29 Antibody (Alexa Fluor 350)

Target: C12ORF29 (Chromosome 12 Open Reading Frame 29 (C12ORF29))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C12ORF29 antibody is conjugated to Alexa Fluor 350

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 C12ORF29

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 C12ORF29

Target: C12ORF29 (Chromosome 12 Open Reading Frame 29 (C12ORF29))

Alternative Name: C12ORF29 (C12ORF29 Products)

Synonyms: C12orf29 antibody, 4930571E09Rik antibody, A730088G13Rik antibody, AW551239 antibody, C430008C19Rik antibody, chromosome 12 open reading frame 29 antibody, chromosome 5 open reading frame, human C12orf29 antibody, chromosome 3 open reading frame, human C12orf29 antibody, RIKEN cDNA 4930430F08 gene antibody, C12orf29 antibody, C5H12orf29 antibody, C3H12orf29 antibody, 4930430F08Rik antibody

Background:

Synonyms: CL029_HUMAN, Uncharacterized protein C12orf29.

Background: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf29 gene product has been provisionally designated C12orf29 pending further characterization.

Gene ID: 91298