epitope mapping near the N-terminus of PNO1 of human origin
Modification Notes
PNO1 (partner of NOB1), also known as KHRBP1, is a 252 amino acid protein that localizes to the nucleolus and contains one KH domain. Expressed in a variety of tissues, including kidney, lung, liver and spleen, with lower levels present in brain, heart, colon and skeletal muscle, PNO1 may play a role in RNA binding events during transcription or translation. The gene encoding PNO1 maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes. Additionally, an extremely rare recessive genetic disorder, Alström syndrome, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of PNO1 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 near the N-terminus of PNO1 of human origin
Tissue Specificity
epitope mapping near the N-terminus of PNO1 of human origin