epitope mapping at the N-terminus of TMEM50B of human origin
Modification Notes
TMEM50B (transmembrane protein 50B), also known as HCV p7-trans-regulated protein 3 (HCVP7TP3), is a 158 amino acid protein belonging to the UPF0220 family. The gene that encodes TMEM50B maps to chromosome 21, the smallest of the human chromosomes. 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.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of TMEM50B of mouse, rat and human origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping at the N-terminus of TMEM50B of human origin
Tissue Specificity
epitope mapping at the N-terminus of TMEM50B of human origin