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Description
C12ORF68 Polyclonal Antibody, Biotin Conjugated. ? Target 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 mor
Immunogen
KLH conjugated synthetic peptide derived from human C12ORF68
Other Names
LOC387856; Uncharacterized protein C12orf68; CL068_HUMAN.