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PR1MA™ RNase Inhibitor
PR1MA™ RNase Inhibitor (RI) is a 50 kDa protein that specifically inhibits RNases A, B, and C by binding noncovalently in a 1:1 ratio at high affinity. It can be used in isothermal amplification and molecular diagnostic assays, cDNA synthesis, and other applications where RNA stability is important. It is ineffective against RNase1, T1, S1 Nuclease, or RNase H. It has no inhibition of polymerase activity when used with Taq DNA polymerase, AMV, M-MuLV, HIV reverse transcriptases, or phage RNA polymerases.
Storage Buffer
- 50% glycerol
- 10 mM Tris-HCl
- 50 mM KCl
- 8 mM DTT
- pH = 7.5
*To prevent the release of ribonuclease from RNase Inhibitor, temperatures greater than 50°C and high concentrations of denaturing reagents such as urea should be avoided.
*These products are intended for research use only, not for therapeutic or diagnostic purposes in humans or animals. The safety and efficacy of these products in diagnostic or other clinical uses has not been established.
REPLACEMENT DF COLUMNS AND COLLECTION TUBES - 100 PACK
- For use with leftover reagents from IBI PCR/Gel Extraction Kits or competitive products
- Sample Size: 300 mg agarose gel/100 µL PCR product
- Elution Volume: 20 to 50 µL
- Binding Capacity: Up to 10 µg
The Replacement DF Columns and Collection Tubes are for use with leftover reagents from IBI PCR/Gel Extraction Kits including the following item numbers: IB47020 and IB47030.
The replacement spin columns and collection tubes can also be used with comparable, competitive PCR/Gel Extraction Kit reagents that utilize a bind, wash, elute method. However, you must observe the sample size, binding capacity, and elution volume for the replacement column stated in the specifications.
SPECIFICATIONS
Sample Size: 300 mg of agarose gel or 100 µL of PCR product
Format: Spin column or vacuum manifold
Expected yield: 90% for Gel extraction and 95% for PCR Clean-up
Elution volume: 20 µL to 50 µL
Operation time: 20 minutes
Purified DNA is ready for use in Fluorescent or Radioactive sequencing, ligation, PCR, restriction enzyme digestion, and DNA labeling.
MagBio HighPrep™ Plant DNA Plus Kit
Magnetic beads based kit designed to extract high-quality genomic DNA from plants (leaves, roots, seeds).
- PCR, Real-time PCR
- Cloning, genotyping
- Sequencing
- Plant breeding
- Purified PCR grade DNA with no inhibiting substances (polysaccharides and phenols)
- Includes beads to homogenize sample
- Eliminate need of grinding
- Adaptable to automation
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IBI 96-Well Vacuum Manifold
- Optimized for use with all of IBI 96-well kits
- The thin upper portion of the manifold is designed to reduce cross contamination
- Allows for the most effective extraction and purification of plasmid DNA, genomic DNA, viral DNA & RNA, total RNA and PCR products
- Materials: Manifold - made of anodized aluminum, Gasket - Ethylene propylene, O-Ring - Silicone
- Dimensions: 17x12x8cm
- Maximum vacuum: Approx. 71cm Hg (28 in Hg) (-13.7psi)
MagBio MagQuant™ Plus DNA V2
Magnetic bead based kit for normalization of DNA concentration, and quantitation of DNA for NGS and other applications
- Next Gen Sequencing library construction
- Amplicon normalization
- Genomic DNA normalization
- PCR, qPCR
- Rapid and reliable quantitation and normalization of DNA
- No centrifugation step, no filtration step
- Eliminates the need for standard curve
- Allowing the processing of pool DNA samples from various sources
- Equilizing input genomic DNA concentration for DNA libray construction to help produce consistent and reliable NGS data without tedious initial input DNA quantitation.
The MagQuant™ Plus DNA V2 Kit utilizes paramagnetic bead-based technology for genomic DNA quantitation and concentration normalization. The DNA normalization occurs during the purification process. Standard methods of DNA quantitation require the use of a standard curve derived from DNA samples of known concentrations; processing DNA samples from various sources would require extensive work and reagent use. MagQuant™ Plus DNA V2‘s proprietary technology allows to obtain a given DNA quantitation and required concentration of DNA samples regardless of the source by adding a specific number of beads to the DNA sample.
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High Throughput PCR Clean-Up
The 96-well PCR Clean-Up/DNA Extraction Kits provide a high-throughput, rapid and economical method to purify DNA fragments. Chaotropic salt is used to denature enzymes and in this condition, DNA fragments are bound by the glass fiber matrix in each well of the plate. Once the contaminants have been removed, the purified DNA is eluted by a low salt elution buffer or water. Salts, enzymes, and unincorporated nucleotides are effectively removed from reaction mixtures without toxic phenol extraction or alcohol precipitation. This entire protocol can be completed in 30-40 minutes, and the eluted DNA is ready to use in restricted digestion, ligation, PCR, and sequencing reactions.
Sample Size: |
Up to 50µl of PCR product |
Format: |
96-Well Plates |
Operation: |
Centrifuge/Vacuum manifold |
Binding Capacity: |
10ug per well |
DNA Size: |
50bp-10kb |
Recovery: |
80-90% for Gel Extraction |
Operation Time: |
30 min for PCR Clean-Up |
MagBio HighPrep™ PCR Clean-up System
Magnetic beads based reagent for manual and automated post-PCR and post-enzymatic reaction clean-up, for NGS library clean-up and reliable amplicon size selection.
Applications
Post-PCR and post-enzymatic reaction clean-up used for/during:
- NGS library preparation
- Amplicon size selection for NGS
- Microarrays
- PCR
- Restriction enzyme digestions, adapter ligations
- Cloning
- Rapid and reliable post-PCR and post enzymatic reaction clean-up
- Efficient wash from contaminants
- High recovery of amplicons >100bp
- Uniform fragments size distribution
- Adaptable to high throughput liquid handling workstations
, Beads
High Throughput PCR Clean-Up
The 96-well PCR Clean-Up/DNA Extraction Kits provide a high-throughput, rapid and economical method to purify DNA fragments. Chaotropic salt is used to denature enzymes and in this condition, DNA fragments are bound by the glass fiber matrix in each well of the plate. Once the contaminants have been removed, the purified DNA is eluted by a low salt elution buffer or water. Salts, enzymes, and unincorporated nucleotides are effectively removed from reaction mixtures without toxic phenol extraction or alcohol precipitation. This entire protocol can be completed in 30-40 minutes, and the eluted DNA is ready to use in restricted digestion, ligation, PCR, and sequencing reactions.
Sample Size: |
Up to 50µl of PCR product |
Format: |
96-Well Plates |
Operation: |
Centrifuge/Vacuum manifold |
Binding Capacity: |
10ug per well |
DNA Size: |
50bp-10kb |
Recovery: |
80-90% for Gel Extraction |
Operation Time: |
30 min for PCR Clean-Up |
fficient Gel Extraction and PCR Clean-up
The Gel/PCR DNA Fragments Extraction Kits are designed to recover or concentrate DNA fragments (50bp-10kb) from agarose gel, PCR reaction, or any other enzymatic reaction. This method uses a chaotropic salt and guanidine thiocyanate to dissolve the agarose gel and denature the enzymes. The DNA fragments in the chaotropic salt are bound to the glass-fiber matrix of the spin column. After washing off the contaminants, the purified DNA fragments are eluted by low salt elution buffer or water. Salts, enzymes, and unincorporated nucleotides can be effectively removed from the reaction mixture without phenol extraction or alcohol precipitation.
Sample: |
up to 300mg agarose gel slice
up to 100µl PCR product or other enzymatic reaction |
Format: |
Spin columns |
Operation: |
Centrifuge/Vacuum Manifold |
Binding Capacity: |
10µg DNA |
Expectant Yield: |
80-90% for gel extraction
90-95% for PCR clean-up |
Operational Time: | 15min. for PCR clean-up/20min. for gel extraction |
Applications: |
PCR, Fluorescent or Radioactive Sequencing, Restriction Digests, DNA Labeling, Ligations |
fficient Gel Extraction and PCR Clean-up
The Gel/PCR DNA Fragments Extraction Kits are designed to recover or concentrate DNA fragments (50bp-10kb) from agarose gel, PCR reaction, or any other enzymatic reaction. This method uses a chaotropic salt and guanidine thiocyanate to dissolve the agarose gel and denature the enzymes. The DNA fragments in the chaotropic salt are bound to the glass-fiber matrix of the spin column. After washing off the contaminants, the purified DNA fragments are eluted by low salt elution buffer or water. Salts, enzymes, and unincorporated nucleotides can be effectively removed from the reaction mixture without phenol extraction or alcohol precipitation.
Sample: |
up to 300mg agarose gel slice
up to 100µl PCR product or other enzymatic reaction |
Format: |
Spin columns |
Operation: |
Centrifuge/Vacuum Manifold |
Binding Capacity: |
10µg DNA |
Expectant Yield: |
80-90% for gel extraction
90-95% for PCR clean-up |
Operational Time: | 15min. for PCR clean-up/20min. for gel extraction |
Applications: |
PCR, Fluorescent or Radioactive Sequencing, Restriction Digests, DNA Labeling, Ligations |
- Sample Size: up to 5×106 cultured animal cells/up to 25mg animal tissue /up to 500µl whole blood/up to 200µl biological fluids (serum, plasma)
- Expectant Yield: up to 9µg of genomic DNA/20µg of total RNA/120µg of protein from 1×106 of HeLa cells
- Operation Time: DNA/RNA purification within 25 minutes, protein precipitation within 50 minutes
- Elution Volume: 50 200µl (genomic DNA)/25 50µl (total RNA)
- Format: genomic DNA spin column and total RNA spin column
IBI DNA/RNA/Protein Extraction Kits
The IBI All Prep DNA RNA Protein Mini Kit provides an efficient method for purifying genomic DNA, total RNA, and total protein simultaneously from cultured cells, animal tissues, whole blood, and biological fluids. Chaotropic salt is used to lyse cells and inactivate DNases and RNases, allowing DNA to bind to the genomic DNA spin column. The flow-through can then be transferred to the RNA Spin column for RNA binding. Contaminants are effectively removed using wash buffers followed by pure genomic DNA elution in a low salt buffer and pure total RNA elution in RNase-free water.
DNA/RNA purification can be completed in 25 minutes without phenol/chloroform extraction or alcohol precipitation, and protein purification can be completed in 50 minutes. The purified DNA, with approximately 20 30Kb, is suitable for use in PCR or other enzymatic reactions and the purified RNA (including miRNA) is ready for use in RT-PCR, Real-Time PCR, northern blotting, primer extension, mRNA selection, and cDNA synthesis. The purified proteins can be directly analyzed on a SDS-PAGE and subsequent western blot.
The quality of the All Prep DNA RNA Protein Mini Kit is tested on a lot-to-lot basis by isolating genomic DNA and total RNA from 1x106 cultured animal cells. The purified DNA and total RNA is quantified with a spectrophotometer and analyzed by electrophoresis on a 1% agarose gel. The purified protein is quantified by Bradford assay analyzed on SDS-PAGE.
Specifications
Sample: Cultured cells, animal tissue, whole blood & biological fluids
Format: Genomic DNA spin column and Total RNA spin column.
Yield: up to 9ug of Genomic DNA / 20ug of Total RNA / 120ug of Protein from 1 x 106 HeLa cells.
Operation Time: Within 25 minutes
Elution volume: 50 200ul for Genomic DNA / 25 50ul for Total RNA.
Simultaneous extraction of Genomic DNA and Total RNA from cultured cells, animal tissues, whole blood and biological fluids.
MagBio HighPrep™ Viral DNA/RNA Kit
- RT-qPCR; RT-PCR, PCR
- One-Step RT-qPCR
- Virus detection, genotyping
- Viral load monitoring,
- OPTIMIZED FOR ISOLATION OF SARS-CoV-2 RNA
- Rapid and reliable purification of viral nucleic acids
- Adaptable to various automated liquid handling workstations
- No toxic organic solvents
The HighPrep™ Viral DNA/RNA kit is designed for rapid and reliable isolation of total viral nucleic acids from whole blood, serum, plasma, saliva and other body fluids as well as nasopharyngeal swabs soaked in virus transport media or other buffers. This kit is highly efficient in vIral nucleic acid isolation and the extracted RNA (and DNA) is suitable for direct use in most downstream applications such as one-step RT-qPCR, RT-PCR, PCR, nucleic acid amplification, cloning, sequencing, and enzymatic reactions. The kit can be used in low throughput manual workflows and is also adaptable to majority of the liquid handling workstations in the market.
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