Influenza Virus A H9N2 Probe Realtime RT-PCR Kit DNA / RNA EXTRACTION & ANALYSISDescription Influenza Virus A H9N2 Probe Realtime RT PCR Kit is a one step RT PCR kit intended for research use in nucleic acid analysis under controlled laboratory conditions using probe based real time PCR. Purified RNA is reverse transcribed into cDNA and subsequently amplified using sequence specific primers and probes. During amplification, fluorescence signals are generated through probe cleavage, allowing real time monitoring of amplification
demonstrating remarkable potential in oncology
Highlands J Virus Probe qRT-PCR Kit is a one-step RT-PCR kit intended for research use in nucleic acid analysis under controlled laboratory conditions using probe-based real-time PCR
and some plant species
Mycobacterium avium subspecies paratuberculosis Probe qPCR Kit is a PCR kit intended for research use in nucleic acid analysis under controlled laboratory conditions using probe-based real-time PCR
Immunohistochemical analysis of paraffin-embedded Human colorectal cancer tissue or SYCE1 antigen-treated (Neutralization experiment) using P114977(SYCE1 Antibody) at dilution 1/55
Granulin/GRN detect Antibody
Bonamia exitiosus Probe qPCR Kit is a PCR kit intended for research use in nucleic acid analysis under controlled laboratory conditions using probe-based real-time PCR
store unused DNA Dilution Buffer at 2–8 °C
Swissprot No Q9NW61 Gene Accession BC003084 WB Predicted band size 18 kDa WB Positive control WB Recommended dilution 500-2000 IHC predicted cell location Predicted cell location: Cytoplasm IHC positive control Positive control: Human esophagus cancer IHC Recommed dilution Recommended dilution: 100-200 Storage
Full name TMEM192 rabbit monoclonal antibody Alternative names 50 μl/100 μl Reactivity rabbit monoclonal Applications WB Host Rabbit Clone type rabbit monoclonal Target Background Enables protein homodimerization activity
Full name BSG rabbit polyclonal antibody Alternative names 50 μl/100 μl Reactivity rabbit polyclonal Applications WB
and inclusion of an internal control
