| FENa, FeNa | Fractional Excretion of Sodium ; Volume의 개념을 제거하여 좀 더 정확한 신장의 농축 능력을 평가, &n... |
|---|---|
| PCR | Polymerase Chain Reaction |
| Pcr | Plasma Creatinine |
| ACD-PCR | active compression-decompression post-compression remodeling |
| PCR | patient contact record; phosphocreatinine; plasma clearance rate; polymerase chain reaction; post-co... |
| CARD | Catalysed Reporter Deposition |
|---|---|
| AP-PCR | Arbitrarily Primed PCR |
| DOP-PCR | Degenerate Oligonucleotide Primed PCR |
| DDRT-PCR | Differential display reverse transcription PCR |
| IS-PCR | In situ PCR |
| genes, reporter | Genes whose expression is easily detectable and therefore used to study promoter activity at many positions in a target genome. In recombinant DNA technology, these genes may be attached to a promoter region of interest. (12 Dec 1998) |
|---|---|
| reporter gene | <molecular biology> A gene that encodes an easily assayed product (e.g. CAT) that is coupled to the upstream sequence of another gene and transfected into cells. The reporter gene can then be used to see which factors activate response elements in the upstream region of the gene of interest. (18 Nov 1997) |
| PCR | <molecular biology, technique> The first practical system for in vitro amplification of DNA and as such one of the most important recent developments in molecular biology. Two synthetic oligonucleotide primers, which are complementary to two regions of the target DNA (one for each strand) to be amplified, are added to the target DNA (that need not be pure), in the presence of excess deoxynucleotides and Taq polymerase, a heat stable DNA polymerase. In a series (typically 30) of temperature cycles, the target DNA is repeatedly denatured (around 90_C), annealed to the primers (typically at 50-60_C) and a daughter strand extended from the primers (72_C). As the daughter strands themselves act as templates for subsequent cycles, DNA fragments matching both primers are amplified exponentially, rather than linearly. The original DNA need thus be neither pure nor abundant and the polymerase chain reaction has accordingly become widely used not only in research, but in clinical diagnostics and forensic science. Acronym: PCR (14 Oct 1997) |
| PCR test | <investigation> A very sensitive test that measures the presence or amount of RNA or DNA of a specific organism or virus (for example: HIV or CMV) in the blood or tissue. PCR tests such as HoffmannLa Roche's HIV RT PCR are being used to gauge HIV disease progression and the effect of particular treatments on HIV infection. (09 Oct 1997) |
| reverse transcriptase PCR | A technique used to amplify RNA targets. The specimen containing the target RNA (e.g., HIV-1 RNA, Hepatitis C Virus RNA) is subjected to reverse transcription to make complementary DNA (cDNA), which is then, in turn, amplified by PCR. Acronym: RT-PCR (05 Mar 2000) |
| differential display PCR | Method of image formation in the light microscope based on the method proposed by Nomarski (though strictly speaking all forms of optical microscopy rely to a greater or lesser extent on differential interference). The light beam is split by a Wollaston prism in the condenser, to form slightly divergent beams polarized at right angles. One passes through the specimen (and is retarded if the refractive index is greater) and one through the background nearby: the two are recombined in a second Wollaston prism in the objective and interfere to form an image. The image is spuriously three dimensional the nucleus, for example: appears to stand out above the cell (or be hollowed out) because it has a higher refractive index than the cytoplasm. The Nomarski system has the advantage that there is no phase halo, but the contrast is low and image formation with crowded cells is poor because the background does not differ from the specimen. (18 Nov 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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