The film Z721530, Excel Scientific AFS-25 AlumaSeal II, with a thickness of 36 um, can serve as an alternative for Z721549 for end users seeking film with a thickness of 38 um or less.
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€115.00
About This Item
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material
aluminum film (medical grade adhesive)
sterility
non-sterile
feature
piercable
packaging
pack of 100 ea
manufacturer/tradename
Excel Scientific F-96-100
technique(s)
PCR: suitable
L
127 mm
W × L
7.8 cm × 12.7 cm
W
78 mm
size
38 μm
application(s)
agriculture
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This Item | Z721557 | A2350 | Z721530 |
|---|---|---|---|
| material aluminum film (medical grade adhesive) | material aluminum film (medical grade adhesive) | material aluminum film | material aluminum film (medical grade adhesive) |
| W × L 7.8 cm × 12.7 cm | W × L 8.25 cm × 13.73 cm | W × L 8.26 cm × 14.61 cm | W × L 8.26 cm × 14.61 cm |
| manufacturer/tradename Excel Scientific F-96-100 | manufacturer/tradename Excel Scientific F-384-100 | manufacturer/tradename Excel Scientific AF-100 | manufacturer/tradename Excel Scientific AFS-25 |
| sterility non-sterile | sterility non-sterile | sterility non-sterile | sterility sterile |
| packaging pack of 100 ea | packaging pack of 100 ea | packaging pkg of one zippered bag of 100 | packaging pack of 50 ea (pkg of one tamper evident bag of 50/box) |
| feature piercable | feature piercable | feature piercable | feature piercable |
General description
- Film dimensions are 127 mm x 78 mm (9.5 mm end tab)
- Available as non-sterile only
- Pierceable
- Recommended temperature range between: -80°C to +120°C
- Certified DNase-, RNase-, and nucleic-acid-free
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Protocols
Reactions using REDTaq® DNA polymerase are formulated as any PCR mixtures. There are no additional reaction preparation steps or protocol changes required.
Protocol for high fidelity amplification of long PCR fragments up to 22kb from complex DNA mixtures and up to 40kb from simple DNA mixtures.
MTP™ Taq DNA Polymerase is a recombinant thermostable enzyme from Thermus aquaticus expressed in E. coli and purified using a proprietary process to minimize levels of contaminating DNA.
Method for amplification of DNA from damaged DNA sources. Particularly useful for DNA extracted from old samples.
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