Tissue cDNA (Matched Pairs), Human Primary Tumor and Normal, Kidney, BioGenomics™
|Cloning||Storage: -20°CShipping: Dry Ice|
BioSelect™ Tissue cDNA: cDNA is supplied as First Strand, Multiple Tissue Panels, and Matched Pairs. PCR-ready First Strand cDNA is tissue specific and are ready-to-use for gene discovery or expression analysis. Over 350 cDNAs from human adult and fetal normal tissues, human diseased and tumor tissues, rat, mouse, monkey and plant tissues are included in this extensive collection.
Human cDNA matched pair products include: Primary Pair (PP), or Primary and Metastatic Pair (PM). PP consists of cDNAs isolated from primary tumor and its adjacent normal tissue; PM consists of cDNAs from primary tumor and corresponding metastatic tumor. cDNAs in each pair are prepared from the same donor. This product line is designed for identifying tumor-specific genes and tumor.
The cDNA pair is comprised of 2 vials each containing 10ul of PCR Ready First Strand cDNA. All cDNAs are made under optimal and consistent conditions, which ensure that representation is maintained from total RNA to cDNA. The First-Strand cDNA is synthesized from RNA isolated from a wide variety of documented normal and tumor tissues. Total RNA used for cDNA synthesis is isolated by modified guanidine thiocyanate techniques.
T5595-0895A Primary Tumor cDNA: 1x10rxn
T5595-0895B Adjacent Normal Tissue cDNA: 1x10rxn
~11ug total RNA was primed by an oligo dT primer and reverse transcribed by MMLV reverse transcriptase in 40ul final volume. RT reaction was stopped by heating at 65°C for 10 minutes. The estimated cDNA concentration is about 2.5ng/ul. 1ul cDNA is sufficient for one PCR reaction.
cDNA in 1X RT buffer (50 mM Tris Cl, pH 8.3, 75mM KCl, 3mM MgCl2, 10mM DTT).
Ready to use for PCR quantification of gene expression
Oligo dT primer used to ensure the entire 3' end of cDNA is present
With some cDNA used as templates, 12kb PCR amplicon was obtained to ensure intact cDNAs
The largest selection of cDNAs from different tissues on the market
Placenta cDNA is included in every panel as an interpanel control
Documentation of tissues' clinical histories available (additional cost)
Economical way to get cDNA from multiple tissues
Immediate PCR amplification of known genes for their expression
Quantification of low copy gene expression in multiple tissues
Identification of tissue-specific expression of target genes
Analysis of gene expression in rare tissues
Verification of genetic mutation
Comparison of a specific gene between different tissues
Analysis of mRNA alternative splicing
1. The integrity of the RNA used for cDNA synthesis is examined by visual inspection for the presence of intact bands of 18s and 28s ribosomal RNA when electrophoresed on a denaturing agarose gel. The quality and purity of total RNA were tested by spectrophotometer. A260/280 is between 1.8 and 2.0 (detetcted in 10mM Tris-Cl, pH 7.5). The ratio of 28S/18S is > 1.
2. The RNA used for cDNA synthesis is treated by DNase I and is tested as DNA free RNA by PCR.
3. The synthesized cDNA was 5” selected to ensure its full length. The cDNA was used as a template for PCR amplification of B-actin gene and an 838 basepair B-actin band was visualized on 2% agarose gel. B-actin control primer is included. It is enough for 10 PCR reactions.
Storage and Stability:
Store at -20ºC Stable for 12 months.
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.