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![Human p53 ELISA Kit [NBP1-91257] - Data for Human p53 Platinum ELISA](http://images.novusbio.com/fullsize/Human-p53-ELISA-Kit-NBP1-91257-img0001.jpg "Human p53 ELISA Kit [NBP1-91257] - Data for Human p53 Platinum ELISA")
![Western Blot: ETS1 associated protein II Blocking Peptide [NBP2-11491PEP] - Western Blot of ETS1 Associated protein II antibody with ETS1 associated protein II Blocking peptide in DiluObuffer.](http://images.novusbio.com/fullsize/ETS1-associated-protein-II--Blocking-Peptide-Western-Blot-NBP2-11491PEP-img0001.jpg "Western Blot: ETS1 associated protein II Blocking Peptide [NBP2-11491PEP] - Western Blot of ETS1 Associated protein II antibody with ETS1 associated protein II Blocking peptide in DiluObuffer.")
![Flow Cytometry: MHC Class II Antibody (P-TH81A5) [NBP2-61033] - Obtained with pig leukocytes](http://images.novusbio.com/fullsize/MHC-Class-II-Antibody-P-TH81A5-Flow-Cytometry-NBP2-61033-img0001.jpg "Flow Cytometry: MHC Class II Antibody (P-TH81A5) [NBP2-61033] - Obtained with pig leukocytes")
![Chromatin Immunoprecipitation: RFXAP Antibody [NBP3-18683] - Figure 1 ChIP results obtained with the antibody directed against RFXAP ChIP assays were performed using NALM cells (a cell line derived from human pre-B leukemia), the antibody against RFXAP and optimized primer sets for PCR. Sheared chromatin from 2 million cells and respectively 5 and 7 ug of antibody were used per ChIP experiment. An anti-flag antibody (lane 2) was used as negative IP control. Figure 1 shows the result of the end-point PCR with primers for HLA_DRA, used as positive control (lower panel) and for HLA_DOB, used a negative PCR control (upper panel).](http://images.novusbio.com/fullsize/RFXAP Antibody-Chromatin Immunoprecipitation-NBP3-18683-img0001.jpg "Chromatin Immunoprecipitation: RFXAP Antibody [NBP3-18683] - Figure 1 ChIP results obtained with the antibody directed against RFXAP ChIP assays were performed using NALM cells (a cell line derived from human pre-B leukemia), the antibody against RFXAP and optimized primer sets for PCR. Sheared chromatin from 2 million cells and respectively 5 and 7 ug of antibody were used per ChIP experiment. An anti-flag antibody (lane 2) was used as negative IP control. Figure 1 shows the result of the end-point PCR with primers for HLA_DRA, used as positive control (lower panel) and for HLA_DOB, used a negative PCR control (upper panel).")
![Sandwich ELISA: PIMT Antibody (3F1) [H00096764-M01] - Detection limit for recombinant GST tagged NCOA6IP is approximately 0.3ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/PIMT-Antibody-3F1-Sandwich-ELISA-H00096764-M01-img0002.jpg "Sandwich ELISA: PIMT Antibody (3F1) [H00096764-M01] - Detection limit for recombinant GST tagged NCOA6IP is approximately 0.3ng/ml as a capture antibody.")
![Sandwich ELISA: MED23 Antibody (4H6) [H00009439-M01] - Detection limit for recombinant GST tagged MED23 is 0.03 ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/MED23-Antibody-4H6-Sandwich-ELISA-H00009439-M01-img0001.jpg "Sandwich ELISA: MED23 Antibody (4H6) [H00009439-M01] - Detection limit for recombinant GST tagged MED23 is 0.03 ng/ml as a capture antibody.")
![Sandwich ELISA: ZHX1 Antibody (5E5) [H00011244-M01] - Detection limit for recombinant GST tagged ZHX1 is approximately 0.03ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/ZHX1-Antibody-5E5-Sandwich-ELISA-H00011244-M01-img0002.jpg "Sandwich ELISA: ZHX1 Antibody (5E5) [H00011244-M01] - Detection limit for recombinant GST tagged ZHX1 is approximately 0.03ng/ml as a capture antibody.")