C12ORF50 antibody (Alexa Fluor 350)

Catalog No. ABIN1405623

Product Details anti-C12ORF50 Antibody (Alexa Fluor 350)

Target: C12ORF50 (Chromosome 12 Open Reading Frame 50 (C12ORF50))

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C12ORF50 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 C12ORF50

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 C12ORF50

Target: C12ORF50 (Chromosome 12 Open Reading Frame 50 (C12ORF50))

Alternative Name: C12ORF50 (C12ORF50 Products)

Synonyms: C12orf50 antibody, MGC134438 antibody, chromosome 1 C12orf50 homolog antibody, chromosome 12 open reading frame 50 antibody, chromosome 5 open reading frame, human C12orf50 antibody, C1H12orf50 antibody, C12orf50 antibody, C5H12orf50 antibody

Background:

Synonyms: C5H12orf50, Chromosome 12 open reading frame 50, chromosome 12 open reading frame 50 ortholog, Hypothetical protein LOC160419, CL050_HUMAN.

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 C12orf50 gene product has been provisionally designated C12orf50 pending further characterization.

Gene ID: 160419