Sentence examples for reaction race from inspiring English sources

PCR = polymerase chain reaction; RACE = rapid amplification of cDNA ends; TS-jPCR = target-selective joint PCR.

Rapid amplification of cDNA ends polymerase chain reaction (RACE PCR) confirmed the existence of three distinct ends, one of which is visible only as an expression drop, another only from poly-adenylation tags, and a third visible from both.

RNase: ribonuclease; SNP: single-nucleotide polymorphism; RT-PCR: reverse-transcriptase polymerase chain reaction; RACE: rapid amplification of cDNA ends; ECP: eosinophil cationic protein; EDN: eosinophil-derived neurotoxin; nt: nucleotide; bp: base pair.

BSA: bovine serum albumin; GST: glutathione S-transferase; IF: intermediate filament; IPTG: Isopropyl-β-D-thiogalactopyranoside; RT-PCR = reverse-transcriptase polymerase chain reaction; RACE: rapid amplification of cDNA ends; cDNA; complementary DNA; SDS: sodium dodecyl sulphate.

nt, nucleotides; bp, basepairs; cDNA, complementary DNA; rRNA, ribosomal RNA; kb, kilobase; mtDNA, mitochondrial DNA; PCR, polymerase chain reaction; RT-PCR, reverse transcriptase polymerase chain reaction; RACE, rapid amplification of cDNA ends; LSU, large subunit; SSU, small subunit; ORF, open reading frame; EST, expressed sequence tag; tmRNA, transfer-messenger RNA; UTR, untranslated region.

The isolates in Cluster IV mainly represent multiple race reaction race 1, race 2, race 4 and race 6. Regardless of the origin, the similarities of race composition between the different zones of India indicated that repeated migration of infected seeds.

To analyze the genomic organization of the murine Ctcfl gene, we cloned the 5' end of the Ctcfl cDNA by a rapid amplification of cDNA ends-polymerase chain reaction (RACE-PCR) procedure, using first choice RACE ready testicular cDNA from Balb/c mice (Ambion) and nested oligos (see Table 4 for sequence).

In this study, full-length cDNAs of SgSQS and SgCAS were cloned by a rapid amplification of cDNA-ends with polymerase chain reaction (RACE-PCR) approach.

We used rapid amplification of cDNA ends-polymerase chain reaction (RACE-PCR) to clone a partial 360 base pair (bp) cDNA representing an endogenous sequence and containing an open reading frame (ORF) fused in frame to the lacZ reporter gene.

Primers 3 and 9 were to amplify the 3′ ends of the cat SIRT1 and SIRT3 cDNA sequences respectively, and primers 4 and 10 were used for 5′ rapid amplification of cDNA ends polymerase chain reaction (RACE-PCR).

DNA fragments of the VH and VL chain genes from single mouse plasma cells were amplified by the rapid amplification of the 5' cDNA ends by polymerase chain reaction (5' RACE-PCR) [ 16].