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IBI High-Speed Mini Plasmid Kit

 

The High-Speed Mini Plasmid Kit isolates plasmid DNA from 1-5ml cultures using alkaline lysis and RNase treatment, ensuring minimal genomic DNA/RNA contamination.

 

Additional Details

The High-Speed Mini Plasmid Kits by IBI Scientific are designed to process a sample size of 1-4 mL of bacterial culture, yielding 20-30 µg for high-copy plasmids and 3-10 µg for low-copy plasmids. With an operation time of 30 minutes or less and a binding capacity of up to 30 µg, these kits offer a rapid and efficient solution for plasmid DNA extraction. Check out our basic guide for plasmid kits for more information.

 

Technical Details

In the presence of a chaotropic salt, the plasmid DNA in the lysate binds to the glass-fiber matrix in the spin column. The contaminants are washed off with an ethanol-based wash buffer. The purified plasmid DNA is eluted by a low salt elution buffer or water. This procedure does not require DNA phenol extraction or alcohol plasmid. Typical yields are 20-30 µg for high-copy numbered plasmids or 3-10 µg for low-copy numbered plasmids. The purified plasmid DNA is ready to use for restriction enzyme digestion, ligation, PCR, or sequencing reactions. The entire procedure can be completed in under 30 minutes.

 

Quality Control

The quality of the High-Speed Plasmid Mini Kit is tested on a lot-to-lot basis, by isolating plasmid DNA from a 4 ml overnight E. coli (DH5α) culture, containing plasmid p Bluescript (A600>2U/mL). Following the purification process, a yield of more than 20 µg is expected and the ratio of A260/A280 is between 1.7-1.9. The purified plasmid (1 µg) is used in EcoRI digestion and checked by electrophoresis.

 

Physical Specifications

High-Speed Mini Plasmid Kit
Format Spin Column
Binding Capacity 30 µg
Culture Input 1-5 mL
Culture Type Cultured bacterial cells
Plasmid Size 1-15 kb
Typical Yield 10-30 µg
Elution Volume 30-100 µl
Operation Time <15 minutes

 

 

Item#:
ASDNARNAKIT10

The I-Blue MINI Plasmid Kit was designed for rapid isolation of plasmid DNA from 1-7 mL of cultured bacterial cells. I-Blue Lysis Buffer (an optional color indicator) is included with the kit in order to prevent common handling errors, ensuring efficient cell lysis and neutralization. A modified alkaline lysis method and RNase treatment are used to obtain clear cell lysate with minimal genomic DNA and RNA contaminants. Typical yields are 20-35 µg for high-copy number plasmid or 3-10 µg for low-copy number plasmid from 4 mL of cultured bacterial cells. DNA phenol extraction or alcohol precipitation is not required and the entire procedure can be completed within 15 minutes. The purified plasmid DNA is ready for use in restriction enzyme digestion, ligation, PCR, and sequencing reactions.

Advantages

  • Sample: 1-7 mL of cultured bacterial cells
  • Yield: Up to 50 µg of pure plasmid DNA
  • Format: Plasmid spin column
  • Operation Time: Within 15 minutes
  • Elution Volume: 30-100 µL
  • Kit Storage: Dry at room temperature (15-25°C) for up to 1 year; PD1 and RNase A mixture should be stored at 2-8°C for up to 6 months

Quality Control
The quality of the I-Blue MINI Plasmid Kit is tested on a lot-to-lot basis by isolating plasmid DNA from a 4 mL overnight E. coli (DH5α) culture containing plasmid pBluescript (A600 > 2 U/mL). Following the purification process, a yield of more than 20 µg is obtained and the A260/A280 ratio is between 1.8-2.0. The purified plasmid DNA (1 µg) is used in EcoRI digestion, and analyzed by electrophoresis.

Kit Components


Component

IB47170

IB47171

IB47172

PD1 Buffer*

1 mL

25 mL

65 mL

PD2 Buffer**

1 mL

25 mL

75 mL

PD3 Buffer

1.5 mL

45 mL

100 mL

I-Blue Lysis Buffer

10 µL

250 µL

650 µL

W1 Buffer

2 mL

45 mL

130 mL

Wash Buffer***
(Add Ethanol)

1 mL
(4 mL)

25 mL
(100 mL)

50 mL
(200 mL)

Elution Buffer

1 mL

6 mL

30 mL

RNase A (50 mg/mL)

Added

100 µL

260 µL

PD Columns

4

100

300

2 mL Collection Tubes

4

100

300

*For IB47171 and IB47172 add provided RNase A to PD1 Buffer then mix by shaking for a few seconds. Check the box on the bottle. PD1 and RNase A mixture should be stored at 2-8°C for up to 6 months. For IB47170 samples, RNase A was already added to PD1.

**If precipitates have formed in PD2 Buffer, warm the buffer in a 37°C water bath, followed by gentle shaking to dissolve.

***Add absolute ethanol (see the bottle label for volume) to Wash Buffer then mix by shaking for a few seconds. Check the box on the bottle. Be sure and close the bottle tightly after each use to avoid ethanol evaporation.

Item#:
ASDNARNAKIT13

The Fast Ion Plasmid Maxi Kit (Endotoxin Free) uses pre-packed anion exchange resin columns to purify plasmid DNA from 100-250 ml of bacterial cultures. Modified alkaline lysis method (1) and RNase treatment are used for obtaining clear cell lysate with minimal genomic DNA and RNA contaminants. Once the plasmid DNA has been bound to the column, the contaminants can be washed off using the wash buffer. Finally, the purified plasmid DNA is eluted by a high salt buffer and precipitated with isopropanol for desalting. The entire procedure can be completed in 120 minutes and the obtained high purity plasmid DNA is suitable for transfection, sequencing reactions, PCR and in-vitro transcription.

Specifications:
Endo Free Midi
Endo Free Maxi
Sample:
50ml culture for high-copy
100ml culture for high-copy
100ml culture for low-copy
250ml culture for low-copy
Yield:
up to 200ug of plasmid DNA
500ug to 1mg of plasmid DNA
Format:
gravity flow
gravity flow
Time:
approx 120 min.
approx 120 min.
Item#:
ASDNARNAKIT12

The 96-Well Genomic DNA Kits are designed for high-throughput purification of total DNA (including genomic, mitochondrial and viral DNA) from whole blood and a variety of animal tissues or cells. This method uses Proteinase K and a chaotropic salt to lyse cells and degrade proteins. DNA in the chaotropic salt is bound by the glass fiber matrix of each well. Once any contaminants have been removed, the purified DNA is eluted by a low salt elution buffer or water. The entire procedure can be completed in 1 hour without phenol extraction or alcohol precipitation. These kits can be used for manual filtration or with robotic handling systems, and purified DNA with approximately 20-30kb is suitable for PCR or other enzymatic reactions.

Sample Size:

Up to 25mg of animal tissues, mouse tails or swabs
cultured animal cells  (up to 1 x 10), bacterial cells (up to 1 x 10) and fungus cells (up to 5 x 10)

Format:

96-Well Plates

Operation:

Centrifuge/Vacuum manifold

Binding Capacity:

Up to 30ug per well

Operation Time:

60 minutes

Item#:
ASDNARNAKIT19

The Genomic DNA Mini Kit for Plants provide a quick and easy method for purifying total DNA (including genomic DNA, mitochondrial and chloroplast DNA) from plant tissue. Samples are disrupted by both grinding in liquid nitrogen and lysis buffer incubation. The lysate is treated with RNase A to degrade RNA and then filtered to remove cell debris and salt precipitates. In the presence of the binding buffer, coupled with chaotropic salt, genomic DNA in the lysate binds to the glass fiber matrix of the spin column. Contaminants are removed using a Wash Buffer (containing ethanol) and the purified genomic DNA is eluted by a low salt Elution Buffer or TE. The procedure does not require DNA phenol extraction or alcohol precipitation, and can be completed in less than 1 hour. The purified genomic DNA is ready for use in PCR, Real-time PCR, Southern Blotting and RFLP.

 

MINI

MAXI

Sample Size:

up to 100mg fresh plant tissue/
25mg of dry plant tissue

up to 1g of fresh plant tissue/
250mg of dry plant tissue

Format:

Spin Column

Spin Column

Expectant Yield:

up to 50µ g DNA

up to 140µ g DNA

Operation Time:

60 min or less

60 min

Item#:
ASDNARNAKIT18

The Genomic DNA Mini Kit for Tissue was designed specifically for purifying total DNA (including genomic, mitochondrial and viral DNA) from a variety of animal tissue, paraffin-embedded tissue, buccal swab and amniotic fluid. The provided micropestle can efficiently homogenize tissue samples to shorten the time in the Lysis Step. Proteinase K and chaotropic salt are used to lyse cells and degrade protein, allowing DNA to be easily bound by the glass fiber matrix of the spin column. Once any contaminants have been removed, using a Wash Buffer (containing ethanol), the purified DNA is eluted by a low salt Elution Buffer or TE. The entire procedure can be completed within 1 hour without phenol/chloroform extraction or alcohol precipitation. The expected yield of genomic DNA is up to 50µg and the purified DNA (with approximately 20-30 Kb) is suitable for use in PCR or other enzymatic reactions.

Sample Size:

Up to 50mg of tissue or 200ul of blood

Format:

Spin Column

Expectant Yield:

up to 50µ g DNA in 50-200µ l

Operation Time:

60 min or less

Item#:
ASDNARNAKIT17

The Genomic DNA Kit for Blood or Cultured Cells provides an efficient method for purifying total DNA (including genomic, mitochondrial and viral DNA) from whole blood, frozen blood, buffy coat, cultured animal/bacterial cells and fungus. Chaotropic salt is used to lyse cells and degrade protein, allowing DNA to bind to the glass fiber matrix of the spin column. Contaminants are removed using a Wash Buffer (containing ethanol) and the purified genomic DNA is eluted by a low salt Elution Buffer or TE. The entire procedure can be completed in 1 hour without phenol/chloroform extraction or alcohol precipitation, with an average DNA yield of 6 µ g from 200 µ l of whole human blood and up to 50µ g of DNA from 200µ l of buffy coat. Purified DNA, with approximately 20-30 Kb, is suitable for use in PCR or other enzymatic reactions.

 

MINI

MAXI

Sample Size:

up to 300µ l fresh whole blood, up to 10 cultured cells

10ml frozen blood, up to 10 cultured cells

Format:

Spin Column

Spin Column

Expectant Yield:

up to 50µ g DNA in 50-200µ l

up to 140µ g DNA in 1-2ml

Operation Time:

40 min or less

60 min or less

Item#:
ASDNARNAKIT16

MagBio HighPrep Viral/Bacterial DNA/RNA Kit


Magnetic beads based kit for rapid isolation of viral and bacterial nucleic acids from whole blood, serum, plasma, saliva and other body fluids. 


Applications

Viral/Bacterial RNA and DNA isolation for:

  •     RT-qPCR; RT-PCR, PCR
  •     One-Step RT-qPCR
  •     Virus detection, genotyping
  •     Viral load monitoring,

Benefits

  •     OPTIMIZED FOR ISOLATION from BACTERIAL & VIRAL samples.
  •     Rapid and reliable purification of nucleic acids
  •     Adaptable to various automated liquid handling workstations
  •     No toxic organic solvents

The HighPrep™ Viral/Bacterial DNA/RNA kit is designed for rapid and reliable isolation of viral & bacterial 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.
Item#:
ASHIHPRPVIRBACDK

Gel Cutting Tips

  • Safely excise bands from gels
  • Avoid cross contamination
  • One-handed operation for quick and accurate gel cutting
  • Safer than using razor blades and won't scratch transilluminators
  • 1.1 x 4 mm
Cut gel with pipet tip on the end of a standard 1000µl pipettor. Gel piece is suspended in tip when pipettor is lifted from the gel. Expel the gel piece by pushing the pushbutton on the pipettor. Tip is ejected in normally using the ejector button.
 
Item#:
ASGELTIP1_1X4
5X RNA Gel Loading Kit
  • Reagents for denaturing and loading RNA samples onto a formaldehyde gel, using MOPS as a buffer
  • RNA sample is dissolved in 10µl of DEPC water and mixed with 35µl of denaturing solution. Heat the sample to 65&#176;C for 5 min. Once the solution has cooled, add 5µl of loading dye. The sample is now ready to load into the gel.
  • DNase/RNase/Protease free
Item#:
IB01015
Your Price:
63.18
Each
6X Loading Dye
    • Used for agarose electrophoresis of DNA, RNA or nucleic acids
    • Contains 3 tracking dyes and 15% Ficoll in a special Tris dye
      • Light blue - around 4000bp in 1% agarose
      • Indigo - around 600bp in 1% agarose
      • Magenta - around 150bp in 1% agarose
    • DNase/RNase/Protease free
Item#:
IB01010
Your Price:
72.26
Each
Discontinued, Contact us for more options!

This brand is being discontinued, please contact us for other options.

Need great dNTPs at a great price? Try our PR1MA™ dNTPs 

 

Bullseye dNTP Mix - 12.5 mM

  • Mix of dATP, dCTP, dGTP, dTTP
  • Each nucleotide is at a concentration of 12.5 mM
  • Ready-to-use molecular grade dNTP solution for use in DNA polymerization, DNA labelling and sequencing processes
  • High purity: >98% by HPLC
  • Supplied in solution at pH 7.5
  • dNTPs are stable at -20°C, avoid multiple freeze/thawing (For long-term usage, aliquoting is recommended)
  • Functionally tested with thermostable polymerases
Item#:
ASPCRDNTP1
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