Agarose, Low Melting point
Agarose, Low Melting point
Description
CleverGEL is a new environmentally friendly agarose suitable for routine analysis of nucleic acids using standard electrophoretic procedures. CleverGEL is manufactured by a process which excludes organic solvents harmful to marine life, making it far kinder to the environment than conventional agarose. A low EEO (electroendoosmotic) flow minimises diffusion so that even the smallest of nucleic acid fragments remains sharp and tightly resolved, while a high gel strength aids handling and maintains compatibility with blotting techniques. CleverGEL is now available in a low melting point form for nucleic acid recovery and enzymatic applications, as well as in a high resolution PCR-grade form to resolve very small nucleic acid fragments 20-800bp in size.
Catalogue Page Number: 29
| SKU | CSL-LMA100 | CSL-LMA5 | CSL-LMA50 |
|---|---|---|---|
| Weight (g) | 100 | 5 | 50 |
| Agarose Type | Low Melting Point | Low Melting Point | Low Melting Point |
| CAS | 39346-81-1 | 39346-81-1 | 39346-81-1 |
| EEO | 0.1 | 0.1 | 0.1 |
| Gelling Point | 26-30C | 26-30C | 26-30C |
| Melting Point | 65C | 65C | 65C |
| Solubility | Clear, colourless @ 2% [w/v] solution | Clear, colourless @ 2% [w/v] solution | Clear, colourless @ 2% [w/v] solution |
| Moisture | 10% | 10% | 10% |
| Gel Strength | >200 g/cm2 (1% [w/v] Gel) | >200 g/cm2 (1% [w/v] Gel) | >200 g/cm2 (1% [w/v] Gel) |
| Nuclease & Protease Free | true | true | true |
This product has been cited in the following research papers:
| Reference title | Date | Citation | Product usage |
|---|---|---|---|
| Impact of mass migrations on the clonal variation of clinical Staphylococcus aureus strains isolated from the Western region of Saudi Arabia | 2018 | Al-Zahrani, I.A., Azhar, E.I., Jiman-Fatani, A.A., Sitdig, L.A., Yasir, M., Al-Ghamdi, A.K. and Harwood, C.R., 2018. Impact of mass migrations on the clonal variation of clinical Staphylococcus aureus strains isolated from the Western region of Saudi Arabia. Journal of infection and public health. | …r all isolates according to the method of Al-Zahrani et al. [12]. Primers were obtained from MWG Biotech (Germany) and the resulting PCR products were separated on 4% low melting point (LMP) agarose (Cleaver Scientific LTD., Warwickshire, UK) in 1 × TBE at 110 V for 3 h. The gels were stained for 15 min in one litre of staining buffer (0.5 μg/ml ethidium bromide in 1 × TBE), destained in tdH2O for… |
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