C12ORF24 Polyklonale Antilichaam, PerCP Vervoeging
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
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
• Rabbit
161-260/273
C12ORF24
• Polyclonal
• IgG
PerCP
KLH conjugated synthetic peptide derived from human C12ORF24
WB, IF (IHC-P)
Purified by Protein A.
482nm/677nm
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
Beschrijving
C12ORF24 Polyklonale Antilichaam, PerCP Vervoeging Beschikbaar in 100 µL. Bestel eenvoudig online met snelle levering.
Specificaties
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