epitope mapping within an internal region of PTD015 of human origin
Modification Notes
With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The PTD015 gene product has been provisionally designated PTD015 pending further characterization.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of PTD015 of human origin and 1810020D17Rik of mouse origin by WB, IP, IF and ELISA non cross-reactive with PTD012 also reactive with additional species, including bovine:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping within an internal region of PTD015 of human origin
Tissue Specificity
epitope mapping within an internal region of PTD015 of human origin
Western blot analysis of PTD015 expression in Hep G2 whole cell lysate.
Application Notes
recommended for detection of PTD015 of human origin and 1810020D17Rik of mouse origin by WB, IP, IF and ELISA non cross-reactive with PTD012 also reactive with additional species, including bovine:
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.