recommended for detection of SERTAD2 of mouse, rat and human origin by WB, IP and ELISA
Modification Notes
SERTAD2 (SERTA domain containing 2), also known as Sei-2 or TRIP-Br2, is a 314 amino acid protein that contains one SERTA domain and functions to integrate the signals provided by transcription factors at E2F-responsive promoters, thereby enhancing the effect of select transcription factors on DNA. Overexpression of SERTAD2 is thought to promote carcinogenesis, suggesting a role for SERTAD2 in tumor formation and metastasis. The gene encoding SERTAD2 maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes. Additionally, an extremely rare recessive genetic disorder, Alström syndrome, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPELISA
WB:1:500~1:2000 IP:1:100~1:500 Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
recommended for detection of SERTAD2 of mouse rat and human origin by WB IP and ELISA
Tissue Specificity
recommended for detection of SERTAD2 of mouse, rat and human origin by WB, IP and ELISA