Human gender is determined by the sex chromosomes X and Y. Pairing two X chromosomes during fertilization leads to female development, and the pairing of an X with a Y chromosome leads to male development. The Y chromosome is the human sex determining chromosome, necessary for male development. Deletion or defect of any gene residing on the Y chromosome is not lethal, however it would impair masculine development and function. Carrying an additional copy of the Y chromosome, as in males with XYY Syndrome, does not lead to an obvious phenotype and most XYY males are unaware of their additional Y chromosome. The Y chromosome contains about 86 genes encoded within approximately 58 million base pairs. The CYorf15B gene product has been provisionally designated CYorf15B pending further characterization.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of CYorf15B of human origin by WB, IP, IF and ELISA non cross-reactive with CYorf15A
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping within an internal region of CYorf15B of human origin
Tissue Specificity
epitope mapping within an internal region of CYorf15B of human origin