Verified by Multiple Cell Samples With an antibody validation through multiple cell lines will further clarify the antibody specificity. |
Antigen Blocking Verified This method is one of the most conventional antibody specificity verification methods. |
Non-conjugated Antibody Blocking Verified One purpose of this verification experiment with unlabeled antibodies is qualifying whether the specificity change after the labelling. |
Fc Receptor Blocking Verified It's always be recommended to do Fc receptors blockade prior to sample staining if your sample contains some special cell types. |
WB,IF and IHC Verified Other applications also provide information on specificity of the antibody. |
The vast majority of monoclonal antibodies were comparable to the classic clones, which had good reputation internationally, in homogeneity, specificity, sensitivity, affinity, etc..
The antibody products in Sino Biological Inc. (SBI) have high affinity and sensitivity performance. They could be effective in very high dilution to recommended concentration in your experiments.
Antibody stability in Sino Biological Inc. (SBI) produced reagents is determined by real-time and real-temperature testing. We can certify the period of time that the antibody has been tested.
So far, there are over 1500 strictly validated antibodies developed in Sino Biological Inc. favorable for Flow Cytometry assay.
Flow cytometry is a method to evaluate cell membrane proteins and intracellular proteins as well as peptides and DNA. The principle behind FACS is an antigen-antibody reaction, with the antibodies being fluorescently labelled. There are three fluorescent proteins (R-PE, APC, and PerCP) conjugated to antibodies. Flow cytometry quantification is carried out with intercalating color labels (without the antibody). Flow cytometry antibodies are widely used in cell counting, cell sorting, biomarker detection and protein engineering.