Tissue, Total RNA, Human Adult Normal, Salivary gland, BioGenomics™

Referencia T5595-7375-10ug

embalaje : 10ug

Marca : US Biological

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T5595-7375 Tissue, Total RNA, Human Adult Normal, Salivary gland, BioGenomics™

Clone Type
Polyclonal
Grade
Molecular Biology Grade
Shipping Temp
Dry Ice
Storage Temp
-70°C

Total RNAs are available from almost 200 different human adult and fetal normal tissues, human diseased and tumor tissues, as well as mouse, rat, and monkey tissues. Total RNAs are provided ready-to-use for Northern blotting, cDNA synthesis, RNA protection, and RNA differential display. |Total RNA isolation is performed using proprietary techniques. Contamination by RNase, genomic DNA polysaccharides, and proteoglycans has been effectively eliminated. The integrity of the total RNAs is assured by checking for a ratio of greater than 1/1 between 28S and 18S ribosomal RNA. We guarantee high efficiency reverse transcription.||Features:|Total RNA isolated from a wide variety of hard to obtain tissues |Decontamination of polysaccharide, proteoglycan, RNase, and genomic DNA |Extensive quality control procedures to ensure high quality |High efficiency reverse transcription |Available documentation of tissues' clinical histories (additional cost)||Applications:|Northern Blotting, RT-PCR, and RACE |cDNA synthesis and cDNA library construction |cDNA probe for profiling study in gene expression |RNA protection and primer extension |RNA display |Purification of mRNA ||Storage Conditions:|Store Total RNA in RNA storage solution at -70ºC

Applications
Form: Supplied as a liquid in RNA Storage Buffer: 0.1% DEPC-treated water with 0.1mM EDTA. No non-specific endonuleases, no nickase, no exonuclease and no RNase detected.||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.
Form
Supplied as a liquid in RNA Storage Buffer: 0.1% DEPC-treated water with 0.1mM EDTA. No non-specific endonuleases, no nickase, no exonuclease and no RNase detected.