Searching journal content for articles similar to Sarkar et al. 2 (4): 318.

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  1. ...protein coding region. Nucleic Acids Res. 19 : 7155 – 7160 . 22.. Sarkar, G., , Turner, R.T. , Bolander. M.E. Sarkar, G., Turner, R.T. and Bolander. M.E. 1993 . Restriction-site PCR: A direct method of unknown sequence retrieval adjacent to a known locus by using universal primers. PCR Methods Applic. 2...
  2. ...) Restriction-site PCR: A direct method of unknown sequence retrieval adjacent to a known locus by using universal primers. PCR Methods Appl. 2 : 318 – 322 . ↵ Schupp I.W. , Schlake T. , Kirschbaum T. , Zachau H.G. , Boehm T. ( 1997 ) A yeast artificial chromosome contig spanning the mouse immunoglobulin kappa...
  3. ...- able by ethidium bromide staining fol- lowing agarose gel electrophoresis. This was too long for full double-stranded PCR sequencing. Restriction mapping of this product revealed a number of blunt- end restriction sites to which a universal blunt-end novel sequence vectorette (Vec3) could be annealed...
  4. ...to a serotonin receptor protein coding region. Nucleic Acids Res. 19 : 7155 – 7160 . 15.. Sarkar, G., , Turner, R.T. , Bolander. M.E. Sarkar, G., Turner, R.T. and Bolander. M.E. 1993 . Restriction-site PCR: A direct method of unknown sequence retrieval adjacent to a known locus by using universal primers. PCR...
  5. ...(program “PhyML,” Guindon et al. 2010), substitution model selection (program “jModelTest”) (Posada 2008), loci chromosomal distribution (program “Circos”) (Krzywinski et al. 2009), and PCR primer design (program “eprimer”) (Rice et al. 2000). A manual explaining how to use the program is available...
  6. ..., Nitschko H, Busch U, Sing A, Ehrhardt A, et al. 2012. Universal real-time PCR for the detection and quantification of adeno-associated virus serotype 2-derived inverted terminal repeat sequences. Hum Gene Ther Methods 23: 18–28. doi:10.1089/hgtb.2011.034 ↵Barrangou R, Horvath P. 2017. A decade of discovery...
  7. ...status and transcription factor occupancy in the Tal1 3′ flanking region. DNase I/ChIP assays were performed in the 416B cell line with either DNase I (black bars), AcK9 (gray bars), or GATA2 (white bars) and analyzed by real-time PCR using primers across a 4-kb segment of the Tal1 locus from +17 to +20...
  8. ..., Robert E. Paull 7 , Jeffrey L. Bennetzen 6 , Jun Wang 2 , 10 , 12 and Shaoling Zhang 1 , 12 1 Centre of Pear Engineering Technology Research, State Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, Nanjing...
  9. ...promoter. All minimally sufficient regulatory region (tn.msrr) plasmids were derived from the Forkhead basal promoter construct (pCES) ( Harafuji et al. 2002 ). Constructs were generated by standard procedures ( Sambrook and Russell 2001 ) using PCR and subcloning. All truncation and deletion constructs...
  10. ...of the 5′ UTR of the mRNA. The sequence of the new human exon 2 is 82% and 81% identical to exon 2 in the sheep and mouse, respectively. To determine whether mRNA containing this new exon 2 was expressed, Southern blot analysis was performed on RT–PCR products generated by a number of permutations of exon...
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