Tissue cDNA, First Strand, Mouse Adult Normal, Brain, 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.
Total RNA used for cDNA synthesis is isolated by modified guanidine thiocyanate techniques. 11ug total RNA was primed by an oligo dT primer and reverse transcribed by MMLV reverse transcriptase in 40ul final volume. RT Reaction stopped by heating at 65°C for 10 minutes.
• Immediate PCR Amplification of known genes.
• Verification of genetic mutation
• Comparison of a specific gene between different tissues.
• Analysis of mRNA alternative splicing Gene cloning and target sequencing.
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 electrophoreses on a denaturing agarose gel. The quality and purity of total RNA were tested by spectro- photometer. A260/280 is between 1.8-2.0 (detected 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. It is tested as DNA free RNA by PCR.
3. The synthesized animal, cDNA was 5’ selected to ensure its full length. The cDNA was used as template for PCR amplification of beta-actin gene and an 838bp beta-actin band was visualized on 1% agarose gel. beta-actin control primer is included. It is enough for 10 PCR reactions. (T5595-0663A)
Storage : Store cDNAs at -20°C
Form: Supplied as a liquid in 1X RT buffer. (1X RT Buffer: 50 mM Tris-Cl, pH 8.3, 75mM KCl, 3mM MgCI2, 10mM DTT).
Unit: 1ul cDNA is good for one PCR reaction.
Donor Informatin: Lot-to-lot specific
Supplied with: T5595-0663A: Tissue, cDNA, First Strand, Mouse Adult Normal, Brain, Actin Control Primer
Control PCR condition:
Ready First Strand cDNA: 1.0ul
10X PCR Buffer: 2.5ul
10mM dNTP: 0.5ul
Control Primers (5uM): 1.0ul
H2O, Nuclease-free: 19.8ul
Taq Polymerase (5u/ul): 0.2ul
Total Volume: 25ul
• 94°C x 2 minutes, 1 cycle.
• 94°C x 30 seconds, 55°C x 30 seconds, 72°C x 30 seconds, 35 cycles.
• 72°C x 5 minutes, 1 cycle. Then hold at 4°C.
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.