NIP3
Ice packs
22.7 pg/mL
adenovirus
54.9-40000 pg/mL
Chemiluminescent
Rattus norvegicus
2 hours, 40minutes
6-11 Business days
Infection immunity
Rattus norvegicus (Rat)
Double-antibody Sandwich
Short term: 4°C; Long term: see manual.
Bcl2/Adenovirus E1B 19kDa Interacting Protein 3
For research use only. Not for diagnostic procedures.
Tissue homogenates, Cell lysates and other biological fluids
ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED
The Stop Solution is acidic. Do not allow to contact skin or eyes.
The kit is manufactured at ISO 9001 and ISO 13485 certified facilities.
Use Rat Bcl2/Adenovirus E1B 19kDa Interacting Protein 3 (BNIP3) ELISA Kit (CLIA) before 8 months
E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays
This assay has high sensitivity and excellent specificity for detection of Bcl2/Adenovirus E1B 19kDa Interacting Protein 3
No significant cross-reactivity or interference between Bcl2/Adenovirus E1B 19kDa Interacting Protein 3 and analogues was observed.
No significant cross-reactivity or interference between Bcl2/Adenovirus E1B 19kDa Interacting Protein 3 and analogues was observed.
Rats are used to make rat monoclonal anti mouse antibodies. There are less rat- than mouse clones however. Rats genes from rodents of the genus Rattus norvegicus are often studied in vivo as a model of human genes in Sprague-Dawley or Wistar rats.
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Bcl2/Adenovirus E1B 19kDa Interacting Protein 3 were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Bcl2/Adenovirus E1B 19kDa Interacting Protein 3 were tested on 3 different plates, 8 replicates in each plate.CV (%) = SD/meanX100;Intra-Assay: CV
The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.