Toolkit/real-time quantitative PCR

real-time quantitative PCR

Assay Method·Research·Since 1996

Also known as: real-time PCR, real time quantitative PCR

Taxonomy: Technique Branch / Method. Workflows sit above the mechanism and technique branches rather than replacing them.

Summary

We have developed a novel "real time" quantitative PCR method.

Usefulness & Problems

Why this is useful

This method measures PCR product accumulation in real time to quantify starting gene copy number. The abstract presents it as a quantitative PCR format with accurate and reproducible readout.; quantitation of gene copies; higher-throughput quantitative PCR assays; closed-tube PCR quantification without post-PCR handling

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This method measures PCR product accumulation in real time to quantify starting gene copy number. The abstract presents it as a quantitative PCR format with accurate and reproducible readout.

Source:

quantitation of gene copies

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higher-throughput quantitative PCR assays

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closed-tube PCR quantification without post-PCR handling

Problem solved

It avoids post-PCR sample handling, which the abstract says helps prevent carry-over contamination and makes assays faster and higher throughput. It also supports quantitation across at least five orders of magnitude.; reduces need for post-PCR sample handling; reduces potential PCR product carry-over contamination; provides accurate and reproducible quantitation over a large dynamic range

Source:

It avoids post-PCR sample handling, which the abstract says helps prevent carry-over contamination and makes assays faster and higher throughput. It also supports quantitation across at least five orders of magnitude.

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reduces need for post-PCR sample handling

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reduces potential PCR product carry-over contamination

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provides accurate and reproducible quantitation over a large dynamic range

Problem links

provides accurate and reproducible quantitation over a large dynamic range

Literature

It avoids post-PCR sample handling, which the abstract says helps prevent carry-over contamination and makes assays faster and higher throughput. It also supports quantitation across at least five orders of magnitude.

Source:

It avoids post-PCR sample handling, which the abstract says helps prevent carry-over contamination and makes assays faster and higher throughput. It also supports quantitation across at least five orders of magnitude.

reduces need for post-PCR sample handling

Literature

It avoids post-PCR sample handling, which the abstract says helps prevent carry-over contamination and makes assays faster and higher throughput. It also supports quantitation across at least five orders of magnitude.

Source:

It avoids post-PCR sample handling, which the abstract says helps prevent carry-over contamination and makes assays faster and higher throughput. It also supports quantitation across at least five orders of magnitude.

reduces potential PCR product carry-over contamination

Literature

It avoids post-PCR sample handling, which the abstract says helps prevent carry-over contamination and makes assays faster and higher throughput. It also supports quantitation across at least five orders of magnitude.

Source:

It avoids post-PCR sample handling, which the abstract says helps prevent carry-over contamination and makes assays faster and higher throughput. It also supports quantitation across at least five orders of magnitude.

Taxonomy & Function

Primary hierarchy

Technique Branch

Method: A concrete measurement method used to characterize an engineered system.

Target processes

No target processes tagged yet.

Implementation Constraints

cofactor dependency: cofactor requirement unknownencoding mode: genetically encodedimplementation constraint: context specific validationoperating role: sensor

The assay requires PCR and a dual-labeled fluorogenic probe identified in the abstract as a TaqMan probe. The abstract does not specify instrument details.; uses a dual-labeled fluorogenic probe

Validation breadth across biological contexts is still narrow. No canonical validation observations are stored yet, so context-specific performance remains under-specified.

Validation

Cell-freeBacteriaMammalianMouseHumanTherapeuticIndep. Replication

Supporting Sources

Ranked Claims

Claim 1comparative advantagesupports1996Source 1needs review

Compared with other quantitative PCR methods, real-time PCR does not require post-PCR sample handling, which helps prevent PCR product carry-over contamination and makes assays faster and higher throughput.

Unlike other quantitative PCR methods, real-time PCR does not require post-PCR sample handling, preventing potential PCR product carry-over contamination and resulting in much faster and higher throughput assays.
Claim 2comparative advantagesupports1996Source 1needs review

Real-time quantitative PCR is extremely accurate and less labor-intensive than current quantitative PCR methods.

Real-time quantitative PCR is extremely accurate and less labor-intensive than current quantitative PCR methods.
Claim 3dynamic rangesupports1996Source 1needs review

Real-time quantitative PCR has a dynamic range for starting target molecule determination of at least five orders of magnitude.

The real-time PCR method has a very large dynamic range of starting target molecule determination (at least five orders of magnitude).
dynamic range 5 orders_of_magnitude
Claim 4mechanismsupports1996Source 1needs review

Real-time quantitative PCR measures PCR product accumulation through a dual-labeled fluorogenic probe identified as the TaqMan probe.

The method measures PCR product accumulation through a dual-labeled fluorogenic probe (i.e., TaqMan Probe).
Claim 5method introductionsupports1996Source 1needs review

The paper introduces a novel real-time quantitative PCR method.

We have developed a novel "real time" quantitative PCR method.
Claim 6performancesupports1996Source 1needs review

The real-time quantitative PCR method provides very accurate and reproducible quantitation of gene copies.

This method provides very accurate and reproducible quantitation of gene copies.
accuracy very accuratereproducibility reproducible

Approval Evidence

3 sources6 linked approval claimsfirst-pass slugs real-time-pcr, real-time-polymerase-chain-reaction, real-time-quantitative-pcr
in a cohort of 64 patients by real time PCR

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Using real time polymerase chain reaction and immunohistochemistry techniques

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We have developed a novel "real time" quantitative PCR method.

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comparative advantagesupports

Compared with other quantitative PCR methods, real-time PCR does not require post-PCR sample handling, which helps prevent PCR product carry-over contamination and makes assays faster and higher throughput.

Unlike other quantitative PCR methods, real-time PCR does not require post-PCR sample handling, preventing potential PCR product carry-over contamination and resulting in much faster and higher throughput assays.

Source:

comparative advantagesupports

Real-time quantitative PCR is extremely accurate and less labor-intensive than current quantitative PCR methods.

Real-time quantitative PCR is extremely accurate and less labor-intensive than current quantitative PCR methods.

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dynamic rangesupports

Real-time quantitative PCR has a dynamic range for starting target molecule determination of at least five orders of magnitude.

The real-time PCR method has a very large dynamic range of starting target molecule determination (at least five orders of magnitude).

Source:

mechanismsupports

Real-time quantitative PCR measures PCR product accumulation through a dual-labeled fluorogenic probe identified as the TaqMan probe.

The method measures PCR product accumulation through a dual-labeled fluorogenic probe (i.e., TaqMan Probe).

Source:

method introductionsupports

The paper introduces a novel real-time quantitative PCR method.

We have developed a novel "real time" quantitative PCR method.

Source:

performancesupports

The real-time quantitative PCR method provides very accurate and reproducible quantitation of gene copies.

This method provides very accurate and reproducible quantitation of gene copies.

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Comparisons

Source-stated alternatives

The abstract contrasts the method with other current quantitative PCR methods that require post-PCR handling and are more labor-intensive.

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The abstract contrasts the method with other current quantitative PCR methods that require post-PCR handling and are more labor-intensive.

Source-backed strengths

very accurate and reproducible quantitation; at least five orders of magnitude dynamic range; faster and higher throughput than other quantitative PCR methods; less labor-intensive than current quantitative PCR methods

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very accurate and reproducible quantitation

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at least five orders of magnitude dynamic range

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faster and higher throughput than other quantitative PCR methods

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less labor-intensive than current quantitative PCR methods

real-time quantitative PCR and Langendorff perfused heart electrical recordings address a similar problem space.

Shared frame: same top-level item type

Strengths here: appears more independently replicated; looks easier to implement in practice.

real-time quantitative PCR and native green gel system address a similar problem space.

Shared frame: same top-level item type

Strengths here: appears more independently replicated; looks easier to implement in practice.

real-time quantitative PCR and sub-picosecond pump-probe analysis of bacteriorhodopsin pigments address a similar problem space.

Shared frame: same top-level item type

Strengths here: appears more independently replicated; looks easier to implement in practice.

Ranked Citations

  1. 1.
    StructuralSource 1Genome Research1996Claim 1Claim 2Claim 3

    Seeded from load plan for claim c1. Extracted from this source document.