epitope mapping within an internal region of PLEKHN1 of human origin
Modification Notes
PLEKHN1 (pleckstrin homology domain containing, family N member 1) is a 663 amino acid phosphoprotein that contains two pleckstrin homology (PH) domains. Conserved in dog, cow, mouse and rat, PLEKHN1 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 1p36.33. As the largest human chromosome, chromosome 1 makes up approximately 8% of the human genome and contains 260 million base pairs encoding 3,000 genes. Numerous diseases are linked to chromosome 1, such as the rare aging disease Hutchinson-Gilford progeria, familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease and Usher syndrome. Aberrations in chromosome 1 also exist 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 PLEKHN1 isoforms 1-3 of human origin by WB, IP, IF and ELISA also reactive with additional species, including canine:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping within an internal region of PLEKHN1 of human origin
Tissue Specificity
epitope mapping within an internal region of PLEKHN1 of human origin