PUSL1 (tRNA pseudouridylate synthase-like 1) is a 303 amino acid protein that belongs to the tRNA pseudouridine synthase truA family. Existing as two alternatively spliced isoforms, the PUSL1 gene is conserved in dog, cow, mouse, rat, chicken, zebrafish, fruit fly, mosquito, A.thaliana and rice, and maps to human chromosome 1p36.33. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are all associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of PUSL1 isoforms 1 and 2 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 within an internal region of PUSL1 of human origin
Tissue Specificity
epitope mapping within an internal region of PUSL1 of human origin