Tissue, Genomic DNA (Matched Pairs), Human Primary Tumor and Metastasis, Liver, BioGenomics™

Biologicals / Biologicals-Tissues-Genomic DNA, Human, Matched Pairs

-20°C

Supplied as a liquid in 1X TE buffer (10mM Tris, pH 8.0, 1mM EDTA).

Genomic DNAs are isolated from over 100 different human and fetal normal tissues, human diseased and tumor tissues, mouse, rat, monkey, and plant tissues. Our genomic DNAs are provided ready to use for SNP analysis, Southern Blotting, and PCR. United States Biological offers almost any genomic DNAs from human, mouse, rat, monkey, and plant tissues; no longer will you need to acquire tissues and isolate genomic DNA by yourself.

Tissue genomic DNAs are isolated from a wide variety of tissues. The genomic DNAs are isolated from tissues by proprietary modified guanidine thiocyanate techniques. The quality and purity of genomic DNA are tested by spectrophotometer and electrophoresis. A260/280 is between 1.8 and 2.0 (detected in 10mM Tris Cl, pH 7.5). Contamination by RNA, polysaccharides and proteoglycans has been effectively eliminated.

T5595-1847 consists of a pair of genomic DNA from primary tumor and corresponding
metastatic tumor. Genomic DNA in each pair is prepared from the same donor. This product line is designed for identifying tumor-specific genes.

Features:
Genomic DNA isolated from a wide variety of hard to obtain tissues
Decontamination of polysaccharide and proteoglycan
Extensive quality control procedures ensure high quality genomic DNA
High efficiency in PCR
Documentation of tissues' clinical histories available

Kit Components:
T5595-1847A: Primary Tumor 1x10ug
T5595-1847B: Metastasis Tumor 1x10ug

Applications:
Suitable for use in SNP analysis, Southern Blot, PCR Genomic DNA library construction and Profiling study in gene expression .

Storage and Stability:
May be stored at 4°C for short-term only. For long-term storage, aliquot and store at -20°C. Aliquots are stable for at least 12 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.