TaqMan™ PreAmp Master Mix Kit
TaqMan™ PreAmp Master Mix Kit
TaqMan™ PreAmp Master Mix Kit
TaqMan™ PreAmp Master Mix Kit
TaqMan™ PreAmp Master Mix Kit
TaqMan™ PreAmp Master Mix Kit
TaqMan™ PreAmp Master Mix Kit
Applied Biosystems™

TaqMan™ PreAmp Master Mix Kit

Stretch your precious samples into more real-time PCR experiments with TaqMan® PreAmp Master Mix Kit. Applied Biosystems® TaqMan® PreAmp MasterLeia mais
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Número do catálogoQuantity
438426740 reactions
Número do catálogo 4384267
Preço (BRL)
9.347,72
Each
Adicionar ao carrinho
Quantity:
40 reactions
Preço (BRL)
9.347,72
Each
Adicionar ao carrinho
Stretch your precious samples into more real-time PCR experiments with TaqMan® PreAmp Master Mix Kit. Applied Biosystems® TaqMan® PreAmp Master Mix Kit contains TaqMan® PreAmp Master Mix and TaqMan® Gene Expression Master Mix. The two work hand in hand to provide a seamless workflow for preamplification and quantitation of mRNA.

The TaqMan® PreAmp Master Mix Kit lets you:

• Amplify cDNA targets equally without introducing bias
• Analyze mRNA from any precious sample such as laser capture microdissections, needle biopsies, and formalin-fixed paraffin-embedded tissues (FFPE)
• Stretch as little as 1 ng of cDNA into 200 real-time PCR reactions for gene expression analysis using TaqMan® Gene Expression Assays
• Analyze up to 100 gene expression targets with minimal hands-on time

Preserves Equilibrium of Targets Without Pre-amplification Bias
In the past, preamplification kits and techniques often resulted in uneven amplification of targets and inaccurate or biased data (as shown by low correlation coefficients between amplified and unamplified samples). TaqMan® PreAmp Master Mix amplifies your small starting samples with no bias and provides extremely high correlation between amplified and unamplified cDNA.

Optimized Workflow and Results
TaqMan® PreAmp Master Mix and TaqMan® Gene Expression Master Mix work in conjunction to provide an optimal workflow for analysis of small starting samples. TaqMan® Gene Expression Master Mix provides reliable quantification over 9 logs of linear dynamic range and has been validated with TaqMan® Assays.
For Research Use Only. Not for use in diagnostic procedures.
Especificações
For Use With (Equipment)7300 System, 7500 Fast System, 7500 System, 7900HT Fast System
Hot StartBuilt-In Hot Start
Passive Reference DyeNo ROX
PolymeraseAmpliTaq Gold DNA Polymerase
Product LineTaqMan
Product TypePreAmp Master Mix Kit
Quantity40 reactions
Sample TypecDNA
Sufficient For200 Reactions
Detection MethodPrimer-probe
GC-Rich PCR PerformanceHigh
PCR MethodqPCR
Reaction SpeedFast or Standard
Unit SizeEach
Conteúdo e armazenamento
Contains 2X TaqMan PreAmp Master Mix (1 mL), TaqMan™ Gene Expression Master Mix (5 mL), and TaqMan™ PreAmp Master Mix Kit Quick Reference Card. Store master mixes at 2-8°C.

Guaranteed minimum shelf life is 60 days (exact expiry date printed on product and CofA).

Frequently asked questions (FAQs)

Can I use preamplification with the TaqMan SNP Genotyping Assays?

There is a preamplification protocol included with our TaqMan Sample-to-SNP Kit. This is designed to work with a lysate sample.

How much template can I start with when using the TaqMan PreAmp Master Mix Kit?

The TaqMan PreAmp Master Mix Kit (P/N 4384267) is intended for use with very small quantities of cDNA (1 to 250 ng). This kit allows you to increase the quantity of specific cDNA targets for gene expression analysis using TaqMan Gene Expression Assays. Starting material is increased prior to PCR and the resulting preamplification product is then used for PCR. The TaqMan PreAmp Master Mix Kit enables multiplex preamplification of up to 100 targets at a time and provides unbiased amplification of specific amplicons for analysis with TaqMan Gene Expression Assays. For more detailed information on this kit, please refer to the TaqMan PreAmp Master Mix Kit Protocol (P/N 4384557).

What is the TaqMan PreAmp Master Mix Kit?

The TaqMan PreAmp Master Mix Kit (P/N 4384267) preamplifies small amounts of cDNA without introducing amplification bias to the sample. Preamplification enables you to stretch your limited sample into many more real-time PCR reactions. TaqMan PreAmp Master Mix Kit consists of TaqMan PreAmp Master Mix and the TaqMan Gene Expression Master Mix. The two work hand in hand to provide the best results in preamplification and quantitation of mRNA.

For more detailed information on this kit, please refer to the TaqMan PreAmp Master Mix Kit Protocol (P/N 4384557).

How does the SuperScript IV Single Cell/Low Input cDNA PreAmp Kit differ from TaqMan PreAmp Master Mix?

TaqMan PreAmp Master Mix is designed for targeted preamplification of up to 100 targets from small amounts of cDNA, while SuperScript IV Single Cell/Low Input cDNA PreAmp Kit allows global preamplification of full-length cDNA from single cells or low input RNA. It provides reagents for cell lysis, reverse transcription and preamplification steps.

Citações e referências (52)

Citações e referências
Abstract
Target genes of neuron-restrictive silencer factor are abnormally up-regulated in human myotilinopathy.
Authors:Barrachina M, Moreno J, Juves S, Moreno D, Olive M, Ferrer I
Journal:Am J Pathol
PubMed ID:17823282
Myotilinopathy is a subgroup of myofibrillar myopathies caused by mutations in the myotilin gene in which there is aggregation of abnormal cytoskeletal proteins and ubiquitin. We report here on the accumulation of neuron-related proteins such as ubiquitin carboxy-terminal hydrolase L1 (UCHL1), synaptosomal-associated protein 25, synaptophysin, and alpha-internexin in aberrant protein ... More
Differential expression of microRNA-675, microRNA-139-3p and microRNA-335 in benign and malignant adrenocortical tumours.
Authors:Schmitz KJ, Helwig J, Bertram S, Sheu SY, Suttorp AC, Seggewiss J, Willscher E, Walz MK, Worm K, Schmid KW
Journal:J Clin Pathol
PubMed ID:21471143
'Background For the clinical management of adrenocortical neoplasms it is crucial to correctly distinguish between benign and malignant tumours. Even histomorphologically based scoring systems do not allow precise separation in single lesions, thus novel parameters are desired which offer a more accurate differentiation. The tremendous potential of microRNAs (miRNAs) as ... More
Deletion of CD14 attenuates Alzheimer's disease pathology by influencing the brain's inflammatory milieu.
Authors:Reed-Geaghan EG, Reed QW, Cramer PE, Landreth GE
Journal:J Neurosci
PubMed ID:21084593
'Alzheimer''s disease (AD) is characterized by the deposition of beta-amyloid (Abeta)-containing plaques within the brain that is accompanied by a robust microglial-mediated inflammatory response. This inflammatory response is reliant upon engagement of innate immune signaling pathways involving the toll-like receptors (TLRs). Studies assessing the roles of TLRs in AD pathogenesis ... More
Anti-epithelial cell adhesion molecule antibodies and the detection of circulating normal-like breast tumor cells.
Authors:Sieuwerts AM, Kraan J, Bolt J, van der Spoel P, Elstrodt F, Schutte M, Martens JW, Gratama JW, Sleijfer S, Foekens JA
Journal:J Natl Cancer Inst
PubMed ID:19116383
'Identification of specific subtypes of circulating tumor cells in peripheral blood of cancer patients can provide information about the biology of metastasis and improve patient management. However, to be effective, the method used to identify circulating tumor cells must detect all tumor cell types. We investigated whether the five ... More
Altered GABAA receptor-mediated synaptic transmission disrupts the firing of gonadotropin-releasing hormone neurons in male mice under conditions that mimic steroid abuse.
Authors:Penatti CA, Davis MC, Porter DM, Henderson LP
Journal:J Neurosci
PubMed ID:20463213
'Gonadotropin-releasing hormone (GnRH) neurons are the central regulators of reproduction. GABAergic transmission plays a critical role in pubertal activation of pulsatile GnRH secretion. Self-administration of excessive doses of anabolic androgenic steroids (AAS) disrupts reproductive function and may have critical repercussions for pubertal onset in adolescent users. Here, we demonstrate that ... More