epitope mapping within an internal region of C5orf24 of human origin
Modification Notes
With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf24 gene product has been provisionally designated C5orf24 pending further characterization.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of C5orf24 isoforms 1 and 2 of mouse and human origin by WB, IP, IF and ELISA non cross-reactive with other C5orf family members also reactive with additional species, including equine, canine, bovine, porcine and avian:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping within an internal region of C5orf24 of human origin
Tissue Specificity
epitope mapping within an internal region of C5orf24 of human origin
Western blot analysis of C5orf24 expression in non-transfected: (A) and human C5orf24 transfected: (B) 293T whole cell lysates.
Application Notes
recommended for detection of C5orf24 isoforms 1 and 2 of mouse and human origin by WB, IP, IF and ELISA non cross-reactive with other C5orf family members also reactive with additional species, including equine, canine, bovine, porcine and avian:
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.