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MP Bio’s thermoluminescent (TLD-XBGN) dosimeter badges measure ionizing radiation and can be used to determine accurate radiation exposure in the workplace. The badge contains four separate thermoluminescent phosphors for calculating tissue equivalence and determining actual doses of radiation. When the phosphors are heated, previously absorbed energy from ionizing radiation exposure is re-emitted in the form of light. The light output is measured, and the dose is calculated. A report is published with a minimal reportable dose of 10mrem.
MP Bio’s thermoluminescent (TLD-XBGN) dosimeter badges measure ionizing radiation and can be used to determine accurate radiation exposure in the workplace. The badge contains four separate thermoluminescent phosphors for calculating tissue equivalence and determining actual doses of radiation. When the phosphors are heated, previously absorbed energy from ionizing radiation exposure is re-emitted in the form of light. The light output is measured, and the dose is calculated. A report is published with a minimal reportable dose of 10mrem.
MP Bio’s thermoluminescent (TLD-XBGN) dosimeter badges measure ionizing radiation and can be used to determine accurate radiation exposure in the workplace. The badge contains four separate thermoluminescent phosphors for calculating tissue equivalence and determining actual doses of radiation. When the phosphors are heated, previously absorbed energy from ionizing radiation exposure is re-emitted in the form of light. The light output is measured, and the dose is calculated. A report is published with a minimal reportable dose of 10mrem.
X-Gal (5-bromo-4-chloro-3-indolyl-ß-D-galactopyranoside) is a ß-galactosidase substrate. In the presence of ß-galactosidase, X-Gal is hydrolyzed and yields a blue precipitate.
TWEEN 20 is a polyoxyethylene sorbitol ester.
Tris is an established basimetric standard and buffer used in biochemistry and molecular biology.
Protein that enhances DNA Polymerase proofreading activity.
Buffer for nucleic acid electrophoresis.
Buffer for nucleic acid electrophoresis.
3 M trisodium citrate solution for use in Southern and northern blotting.
SDS is an anionic detergent typically used to solubilize and denature proteins for electrophoresis. Most proteins bind SDS in a ratio of 1.4 grams SDS to 1 gram protein. The charges intrinsic to the protein become insignificant compared to the overall negative charge provided by the bound SDS.It is RNAse,DNAse, Protease free with an assay value of 20%.This solution is provided as a convenient ready-to-use firmat which eliminates the need to handle powdered SDS.
Ready to use mixture of chloroform and isoamyl alcohol for phebol-based nucleic acid extractions.
20xSSC solution for use in Southern and northern blotting.
Hybridization solution containing 50% formamide and 2X SSC.
10X Phosphate-Buffered Detergent.
Non-alkaline, non-corrosive and non-carcinogenic cleansing solution
Ready-to-use for eliminating DNA from any surface around PCR workstation
Stable and heat resistant
Contains a surfactant plus an agent that destroys DNA
Ready to use 25 mM dNTP mix.