epitope corresponding to amino acids 676-770 mapping at the C-terminus of SPR-5 of C. elegans origin
Modification Notes
Presenilins are components of a protease complex that functions to cleave Notch receptors and the Amyloid precursor protein implicated in Alzheimer’s disease. Mutations in Presenilin 1 and Presenilin 2 are the most common cause of familial early-onset Alzheimer’s disease. A mutation in the Sel-12 presenilin protein is associated with a highly penetrant egg-laying defect caused by a reduction in Notch signaling. The transgenic expression of HOP-1 can rescue a SEL-12 mutant from the egg-laying defect. SPR-5 (suppressor of presenilin defect family member 5) is a 770 amino acid protein that, when mutated, efficiently suppresses the egg-laying defect of the SEL-12 mutant by releasing the repression of HOP-1 expression during developmental stages. SPR-5 is similar to the mammalian PAO protein and is believed to associate with SPR-1, a C. elegans homolog of CoREST-like co-repressor complex that functions in transcriptional repression.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of SPR-5 of ce origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to amino acids 676-770 mapping at the C-terminus of SPR-5 of C. elegans origin
Tissue Specificity
epitope corresponding to amino acids 676-770 mapping at the C-terminus of SPR-5 of C. elegans origin
Application Notes
recommended for detection of SPR-5 of ce origin by WB, IP, IF and ELISA:
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.