Searching journal content for articles similar to Uberla et al. 1 (2): 136.

Displaying results 1-10 of 34
For checked items
  1. .... and Blankenstein. T. 1991 . Generation of competitor DNA fragments for quantitative PCR. PCR Methods Applic. 1 : 136 – 139 . 3.. Stieger, M., , Demolliere, C. , Ahlborn-Laake, L. , Mous. J. Stieger, M., Demolliere, C. Ahlborn-Laake, L. and Mous. J. 1991 . Competitive polymerase chain reaction assay...
  2. ...the precursor of NF-kappa B p50 mRNA in mouse intestine: Quantitative analysis by competitive PCR. Biochim. Biophys. Acta 1215 : 157 – 162 . Thomas, P.S. 1980 . Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc. Natl. Acad. Sci. 77 : 5201 – 5205 . Williams, S., C. Schwer...
  3. ...to be used in the competitive RT-PCR (cRT- PCR) was obtained. Similarly, rapid methods to construct DNA competitors using either PCR and site-directed mu- tagenesis by overlap extension (37) or am- plification of two fragments whose sub- sequent ligation supplies an internally truncated competitor (43) have...
  4. ...the addition of equal amounts of competitor DNA fragments to the probes to be co- amplified during PCR reaction. (1-3) As the competitor fragments are added in equal amounts they should yield equal amounts of PCR products. If the frag- ments derived from mRNA and the com- petitor are distinguishable in size...
  5. ...by usage of novel competitor DNA constructs in quantitative polymerase chain reaction. J. Exp. Med. 174 : 1259 – 1262 . 5. Siebert, P.D. and Larrick. J.W. 1993 . PCR mimics: Competitive DNA fragments for use as internal standards in quantitative PCR. BioTechniques 14 : 244 – 249 . 6. Fandrey, J. and Bunn...
  6. .... , Diamanstein, T. , Blankenstein. T. Uberla, K., Platzer, C. Diamanstein, T. and Blankenstein. T. 1991 . Generation of competitor DNA fragments for quantitative PCR. PCR Methods Applic. 1 : 136 – 139 . 33.. Zack, J.A., , Arrigo, S.J. , Weitsman, S.R. , Go, A.L. , Haislip, A. , Chen. I.S.Y. Zack, J.A., Arrigo, S...
  7. ...(TA Cloning Sys- tem; Invitrogen, San Diego, CA) and FIGURE 4 Dilution series of a 219-bp PCR fragment, stained either with SYBR Green I (A) or ethidium bromide (B). 100 fg competitor RNA (-5• 10S/molecules) was reverse transcribed, Vso of the cDNA was used for PCR (30 cycles). 1 O.1 PCR product...
  8. ...with antisense competitors. BioTechniques 17 : 934 – 942 . 16.. Porcher, C., , Malinge, M.C. , Picat, C. , Grandchamp. B. Porcher, C., Malinge, M.C. Picat, C. and Grandchamp. B. 1992 . A simplified method for determination of specific DNA or RNA copy number using quantitative PCR and an automatic DNA sequencer...
  9. ...templates. This assay offers the high sensitivity of ELCL detection of PCR product coupled with the ability to distinguish product mole- cules by way of a unique restriction site contained within the competitor tem- plate. These properties allow for the quantitative detection of low amounts of target DNA...
  10. ...for quan- titation of cDNA by PCR-based meth- ods, (1-4) most of them utilizing the prin- ciple of competitive PCR (C-PCR) in which a synthetic DNA fragment is co- amplified with the target cDNA seg- ment. We were interested in comparing the expression of cytokine genes in umer- ous samples of antigen...
For checked items

Preprint Server