FroggaBio USA Inc - GenepHlow GelPCR Kit
Theandnbsp;GenepHlowandtrade;andnbsp;Gel Extraction Kit and PCR Cleanup Kitandnbsp;was designed to recover or concentrate DNA fragments from agarose gel, PCR or other enzymatic reactions
Product description | Catalog # | Quantity | Price | |
---|---|---|---|---|
DFH004 |
|
$30.23 $29.85 |
||
DFH100 |
|
$190.00 |
||
DFH300 |
|
$275.00 |
FroggaBio USA Inc - GenepHlow GelPCR Kit Product Description
Theandnbsp;GenepHlowandtrade;andnbsp;Gel Extraction Kit and PCR Cleanup Kitandnbsp;was designed to recover or concentrate DNA fragments from agarose gel, PCR or other enzymatic reactions
The GenepHlow™ Gel Extraction Kit and PCR Cleanup Kit was designed to recover or concentrate DNA fragments from agarose gel, PCR or other enzymatic reactions
This gel extraction kit and PCR cleanup kit includes a pH indicator which is premixed with the binding buffer to ensure optimal pH, facilitate DNA binding and allow for easy observation of undissolved agarose gel
- If pH exceeds the optimal level (>75), the color of the solution will appear purple instead of yellow
-
- 3M Sodium Acetate (pH50), which is included with the kit, can then be added to the solution to adjust pH and return the color to yellow
-
- Chaotropic salt is used to dissolve agarose gel and denature enzymes
-
- DNA fragments in the chaotropic salt are bound by the glass fiber matrix of the spin column
-
- Contaminants are removed with a Wash Buffer (containing ethanol) and the purified DNA fragments are eluted by a low salt Elution Buffer, TE or water
-
- The pH indicator, salts, enzymes and unincorporated nucleotides can be effectively removed from the reaction mixture without phenol extraction or alcohol precipitation and the purified DNA is ready for use in subsequent reactions
-
Applications
- Fluorescent and Radioactive Sequencing
-
- PCR
-
- Restriction Enzyme Digestion
-
- DNA Labeling and Ligation
-
- Microarray
-
- Transfection
-
This gel extraction kit and PCR cleanup kit includes a pH indicator which is premixed with the binding buffer to ensure optimal pH, facilitate DNA binding and allow for easy observation of undissolved agarose gel
- If pH exceeds the optimal level (>75), the color of the solution will appear purple instead of yellow
-
- 3M Sodium Acetate (pH50), which is included with the kit, can then be added to the solution to adjust pH and return the color to yellow
-
- Chaotropic salt is used to dissolve agarose gel and denature enzymes
-
- DNA fragments in the chaotropic salt are bound by the glass fiber matrix of the spin column
-
- Contaminants are removed with a Wash Buffer (containing ethanol) and the purified DNA fragments are eluted by a low salt Elution Buffer, TE or water
-
- The pH indicator, salts, enzymes and unincorporated nucleotides can be effectively removed from the reaction mixture without phenol extraction or alcohol precipitation and the purified DNA is ready for use in subsequent reactions
-
Applications
- Fluorescent and Radioactive Sequencing
-
- PCR
-
- Restriction Enzyme Digestion
-
- DNA Labeling and Ligation
-
- Microarray
-
- Transfection
-
- If pH exceeds the optimal level (>75), the color of the solution will appear purple instead of yellow
- 3M Sodium Acetate (pH50), which is included with the kit, can then be added to the solution to adjust pH and return the color to yellow
- Chaotropic salt is used to dissolve agarose gel and denature enzymes
- DNA fragments in the chaotropic salt are bound by the glass fiber matrix of the spin column
- Contaminants are removed with a Wash Buffer (containing ethanol) and the purified DNA fragments are eluted by a low salt Elution Buffer, TE or water
- The pH indicator, salts, enzymes and unincorporated nucleotides can be effectively removed from the reaction mixture without phenol extraction or alcohol precipitation and the purified DNA is ready for use in subsequent reactions
-
- Fluorescent and Radioactive Sequencing
- PCR
- Restriction Enzyme Digestion
- DNA Labeling and Ligation
- Microarray
- Transfection
-
Applications
Specifications
Format: Spin Column
Binding Capacity: 200 µg
Sample: Agarose Gel SlicePCR Product
Fragment Size: 70 bp-20 kb
pH Indicator: Yes
Recovery: Up to 95%
Elution Volume: 20-50 µl
Operation Time:<20 minutes
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