epitope mapping within an internal region of C21orf62 of human origin
Modification Notes
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf62 gene product has been provisionally designated C21orf62 pending further characterization.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of C21orf62 of human origin, 4932438H23Rik of mouse origin and the corresponding rat homolog by WB, IP, IF and ELISA also reactive with additional species, including porcine and avian:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping within an internal region of C21orf62 of human origin
Tissue Specificity
epitope mapping within an internal region of C21orf62 of human origin
Western blot analysis of C21orf62 expression in SK-N-MC (A), HeLa (B), MIA PaCa-2 (C), KNRK (D) and MES-SA/Dx5 (E) whole cell lysates.
Application Notes
recommended for detection of C21orf62 of human origin, 4932438H23Rik of mouse origin and the corresponding rat homolog by WB, IP, IF and ELISA also reactive with additional species, including porcine and avian:
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.