cell
One 96-Well Plate
CB5002
530 EUR
cell
6 Months
14-3-3 ζ
> 5000 Cells
Research use only
Colorimetric 450 nm
Cell Lysate, Serum, Plasma
Non-Phospho Cell-Based ELISA
Store the entire kit at 4°C upon arrival.
ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED
For cells, cell lines and tissues in culture till half confluency.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
To order 14-3-3 ζ Colorimetric Cell-Based ELISA Kit, please use the cat '' CB5002 '' and submit your purchase order by email or by Fax, please contact us by email or Live chat.
Mitochondrial import stimulation factor S1 subunit; 14-3-3 protein zeta/delta; 1433Z; 143Z; FAS; Factor activating exoenzyme S; KCIP-1; Protein kinase C inhibitor protein-1; YWHAZ
Colorimetric assays or detection use UV absorption or enzymatic color reaction.E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays
14-3-3 ζ Colorimetric Cell-Based ELISA Kit is able to recognize, detecte and quantificate the endogenous levels of both recombinant and naturally produced 14-3-3 ζ proteins, within any experimental sample including cell lysates, serum and plasma.
14-3-3 ζ Colorimetric Cell-Based ELISA Kit is produced by Assay Biotech Company. It's also identified by the synonym '' Mitochondrial import stimulation factor S1 subunit or 14-3-3 protein zeta/delta '' that is able to recognize, detecte and quantificate the endogenous levels of both recombinant and naturally produced 14-3-3 ζ proteins, within any experimental sample including cell lysates, serum and plasma. It's has a colorimetric 450 nm as a detection method, within the range of > 5000 Cells. and that is an appropriate, lysatefree, high throughput and high sensitivity assay kit that can check Human RAGEprotein and its expression profile in cells. This kit can be used in order to measur with a hight precision the relative amounts of Human RAGEinsid the cultured cells as well as detection of the effects that various inhibitors or treatments (ie. siRNA or chemicals), or activators have on Human RAGE.