RNA Save

Tissue and cells storage solution for RNA stabilization
Name SKU Size Price Qty
RNA Save 01-891-1B 100 mL
$45.00

Description

Details

Product Overview:

RNA Save is an aqueous, non toxic, tissue and cells storage solution intended for the preservation of RNA for later isolation. It is a preservation solution that allows recovery of intact RNA from tissues. Samples in RNA Save solution can be stored indefinitely at -20°C or -80°C with no RNA degradation. RNA save solution can be used for the storage of tissues, cells, bacteria and yeasts. The solution may not be effective for the storage of waxy plant tissue and bone because of poor penetration of the solution. RNA Save is compatible with most RNA isolation methods.

Specifications

Specifications

Storage Conditions RT
Shipping Conditions RT
Specifications RNA Save should be stored at room temperature. If precipitation is seen, warm the solution to 37°C and mix carefully for resolubilization.

References

references

  1. K. Luo et al. Identification of interleukin‐16 (IL‐16) and interleukin‐17D (IL‐17D) genes from Dabry's sturgeon (Acipenser dabryanus). Journal of Applied Ichthyology, https://doi.org/10.1111/jai.13769, 2018
  2. K Luo et. al. Analysis of the expression patterns of the cytokine receptor family B (CRFB) and interferon gamma receptor (IFNGR) in Dabry's sturgeon (Acipenser dabryanus). Developmental & Comparative Immunology, volume 84, July 2018, pages 420-426
  3. S. Zhang et al. Characterization and expression analysis of g- and c-type lysozymes in Dabry's sturgeon (Acipenser dabryanus). Fish & Shellfish Immunology, Volume 76, May 2018, pages 260-265
  4. H.A Hassan. Potential mediators of in ovo delivered double stranded (ds) RNA-induced innate response against low pathogenic avian influenza virus infection. Virology Journal 201815:43
  5. A. Amarasinghea et. al. Induction of innate host responses characterized by production of interleukin (IL)-1β and recruitment of macrophages to the respiratory tract of chickens following infection with infectious bronchitis virus (IBV). Veterinary Microbiology, Volume 215, February 2018, Pages 1-10
  6. M. Grinbla et. al. Stylophora pistillata in the Red Sea demonstrate higher GFP fluorescence under ocean acidification conditions. Coral Reefs (2018) 37: 309
  7. M.S. Abdul-Cade et al. In ovo CpG DNA delivery increases innate and adaptive immune cells in respiratory, gastrointestinal and immune systems post-hatch correlating with lower infectious laryngotracheitis virus infection. PLoS ONE 13(3): e0193964. https://doi.org/10.1371/journal.pone.0193964 (2018)
  1. D. Landau et. al. The hypoxia inducible factor/erythropoietin (EPO)/EPO receptor pathway is disturbed in a rat model of chronic kidney disease related anemia. PLoS ONE 13(5): e0196684. https://doi.org/ 10.1371/journal.pone.0196684
  2. I. Simitsidellis et al. A Role for Androgens in Epithelial Proliferation and Formation of Glands in the Mouse Uterus. Endocrinology, Volume 157, Issue 5, 1 May 2016, Pages 2116–2128
  3. Y. Eldar-Yedidia et. al. Low Interferon Relative-Response to Cytomegalovirus Is Associated with Low Likelihood of Intrauterine Transmission of the Virus. PLoS ONE 11(2): e0147883. doi:10.1371/journal.pone.0147883
  4. D. Lizuka et. al. Hepcidin-2 in mouse urine as a candidate radiation-responsive molecule. Journal of Radiation Research, Volume 57, Issue 2, 1 March 2016, Pages 142–149
  5. V.R. Reddy et. al. Hypermethylation of Promoter Region of LATS1 - a CDK Interacting Protein in Oral Squamous Cell Carcinomas - a Pilot Study in India. Asian Pacific Journal of Cancer Prevention, Vol 16, 2015, pages 1599-1603

Documentation

Materials Safety Data Sheet

Manuals and Protocols

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