C12ORF24 Polyklonale Antilichaam, AbBy FluorTM 405 Vervoeging

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 C12orf24 gene product has been provisionally designated C12orf24 pending further characterization.

Chromosome 12 open reading frame 24; HSU79274; Hypothetical protein LOC29902; Protein predicted by clone 23733; F216A_HUMAN; Protein FAM216A; FAM216A.

29902

Q8WUB2

161-260/273

C12ORF24

AbBy Fluor™ 405

KLH conjugated synthetic peptide derived from human C12ORF24

WB, IF (IHC-P)

Purified by Protein A.

401nm/421nm

1µg/µl

WB (1:300-5000), IF (IHC-P) (1:50-200)

Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Unmodified

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

29902

Human, Mouse, Rat, Cow, Sheep, Rabbit