Introduction

The ChargeSwitch® gDNA Mini and Micro Tissue Kits allow rapid and efficient purification of genomic DNA from mini (10-25 mg) or micro (3-5 mg) quantities of tissue, respectively. After preparing the lysates, you may purify DNA in less than 15 minutes using the ChargeSwitch® Technology.
 
Intended Use for the Kits

The ChargeSwitch® gDNA Tissue Kits are designed to allow isolation of genomic DNA from the following sources. The purified genomic DNA is suitable for use in downstream applications including PCR, restriction enzyme digestion, and Southern blotting.

  • Micro-Tissue Kit: Purifies up to 5 µg of genomic DNA from 1-2 mm diameter mouse ear clips or 3-5 mg of tissue. This sample size is suitable for genomic DNA purification from micro-dissected or laser capture micro-dissected samples.
  • Mini-Tissue Kit: Purifies up to 30 µg of genomic DNA from 0.5 cm mouse tail tips or approximately 25 mg of tissue. For spleen tissue, reduce tissue size to 10 mg.


Advantages

Use of the ChargeSwitch® gDNA Tissue Kits to isolate genomic DNA provides the following advantages:

  • Uses a magnetic bead-based technology to isolate genomic DNA without the need for hazardous chemicals, centrifugation, or vacuum manifolds
  • Rapid and efficient purification of genomic DNA from micro or mini quantities of tissue in less than 15 minutes following sample preparation and lysis
  • Simple lysis of tissues with Proteinase K without the need for any mechanical lysis
  • Minimal contamination with RNA
  • The purified genomic DNA demonstrates improved downstream performance in applications including PCR, restriction enzyme digestion, and Southern blotting.


System Specifications

                                                  Mini-Tissue        Micro-Tissue
Starting Material:                       10-25 mg               3-5 mg
Elution Volume:                          250 µl                    150 µl
DNA Yield:                                 Up to 30 µg           Up to 5 µg
DNA Size:                                  > 20 kb                  > 20 kb
 
The ChargeSwitch® Technology

The ChargeSwitch® Technology (CST ®) is a novel magnetic bead-based technology that provides a switchable surface charge dependent on the pH of the surrounding buffer to facilitate nucleic acid purification. In low pH conditions, the CST® beads have a positive charge that binds the negatively charged nucleic acid backbone (see figure below). Proteins and other contaminants are not bound and are simply washed away in an aqueous wash buffer. To elute nucleic acids, the charge on the surface of the bead is neutralized by raising the pH to 8.5 using a low salt elution buffer (see figure below). Purified DNA elutes instantly into this elution buffer, and is ready for use in downstream applications.

 




ChargeSwitch® Magnetic Bead Specifications

Bead Binding Capacity:      5-10 µg genomic DNA per mg
Bead Size:                             < 1 µm
Bead Concentration:           25 mg/ml
Storage Buffer:                     10 mM MES, pH 5.0, 10 mM      NaCl, 0.1% Tween 20
 
Experimental Outline
 
Introduction

The figure below illustrates the basic steps necessary to purify genomic DNA from tissues using the ChargeSwitch® gDNA Tissue Kits.

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Materials

Types of Kits

This manual is supplied with the following products.

ProductCatalog no
ChargeSwitch® gDNA Micro Tissue KitCS11203
ChargeSwitch® gDNA Mini Tissue KitCS11204


Shipping and Storage

All components of the ChargeSwitch® gDNA Tissue Kits are shipped at room temperature. Upon receipt, store the Proteinase K and RNase A at 4° C. Store all other components at room temperature.
 
All components are guaranteed stable for 6 months if stored properly.
 
Contents

The components supplied in the ChargeSwitch® gDNA Tissue Kits are listed below. The reagents supplied are sufficient to perform 25 (Mini Tissue) or 50 (Micro Tissue) purifications.
 
Note:   Some reagents in the kit may be provided in excess of the amount needed.

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Component
Amount
 
Mini Tissue
Micro Tissue
ChargeSwitch® Lysis Buffer (L13)
50 ml
--
ChargeSwitch® Lysis Buffer (L15)
--
50 ml
ChargeSwitch ® Magnetic Beads
3 x 1 ml
2 x 1 ml
Proteinase K (20 mg/ml in 50 mM Tris-HCl, pH 8.5, 5 mM CaCl2, 50% glycerol)
500 µl
500 µl
RNase A (5 mg/ml in 10 mM Tris-HCl, pH 8.5, 10 mM EDTA)
250 µl
250 µl
ChargeSwitch® Purification Buffer (N5)
10 ml
10 ml
ChargeSwitch® Wash Buffer (W12)
50 ml
100 ml
ChargeSwitch® Elution Buffer (E5; 10 mM Tris-HCl, pH 8.5)
10 ml
10 ml
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Ordering Information

Sku Name Size Price Qty
CS11203 ChargeSwitch® gDNA Micro Tissue Kit 50 preps USD 228.00
CS11204 ChargeSwitch® gDNA Mini Tissue Kit 25 preps USD 80.00

General Information

User Supplied Materials

In addition to the reagents supplied with the kit, you will need to have the following materials on hand before beginning:

  • A magnetic separation rack suitable for use with 1.5 ml microcentrifuge tubes (see below)
  • Sterile, 1.5 ml microcentrifuge tubes
  • Vortex mixer
  • 20 µl, 200 µl, and 1 ml sterile, pipette tips
  • Water bath at 55° C


MagnaRack™

The MagnaRack™ available from Invitrogen (Catalog no. CS15000) is a two-piece magnetic separation rack for use in protocols with magnetic beads. The MagnaRack™ consists of a magnetic base station and a removable tube rack. The tube rack can hold up to 24 microcentrifuge tubes. The tube rack fits onto the magnetic base station in two different positions, associating the row of 12 neodymium magnets with a single row of 12 tubes for simple ‘on the magnet’ and ‘off the magnet’ sample processing (see figure below). For more information, see www.invitrogen.com or call Technical Service.





Safety Information

Follow the safety guidelines below when using the ChargeSwitch® gDNA Tissue Kit.

  • Treat all reagents supplied in the kit as potential irritants.
  • Always wear a suitable lab coat, disposable gloves, and protective goggles.
  • If a spill of the buffers occurs, clean with a suitable laboratory detergent and water. If the liquid spill contains potentially infectious agents, clean the affected area first with laboratory detergent and water, then with 1% (v/v) sodium hypochlorite or a suitable laboratory disinfectant.


Handling the ChargeSwitch® Magnetic Beads

Follow the guidelines below when handling the ChargeSwitch® magnetic beads.

  • Do not freeze the beads as this irreparably damages them. Store the beads at room temperature.
  • Always keep the beads in solution. Do not allow them to dry out as this renders them non-functional.
  • When using the beads, resuspend thoroughly in the storage buffer by vortexing before removal.
  • Discard beads after use. Do not reuse.


Elution Buffer

ChargeSwitch® Elution Buffer (E5; 10 mM Tris-HCl, pH 8.5) is supplied with the kit for eluting the DNA from the ChargeSwitch® Magnetic Beads. For best results, use Elution Buffer (E5) to elute the DNA. Alternatively, TE Buffer, pH 8.5-9.0 is acceptable. Note that the pH must be between 8.5-9.0 otherwise the DNA will not elute. Do not use water for elution.
 
The protocol recommends eluting the genomic DNA in 150 µl (Micro Kit) or 250 µl (Mini Kit) of ChargeSwitch® Elution Buffer (E5). You may vary the amount of ChargeSwitch® Elution Buffer (E5) used to obtain genomic DNA in the desired final concentration. For best results, always use a volume of ChargeSwitch® Elution Buffer (E5) that is equal to or greater than the volume of ChargeSwitch® Magnetic Beads used in the protocol. If the volume of ChargeSwitch® Elution Buffer (E5) is lower than the volume of beads used, DNA elution is incomplete. You may need to perform a second elution to recover all DNA.  

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Isolating Genomic DNA Using the Micro Tissue Kit

Introduction

This section provides guidelines and instructions to isolate genomic DNA from micro quantities of tissue using the ChargeSwitch® gDNA Micro Tissue Kit (Catalog no. CS11203).
 
Starting Material

Use this procedure to isolate genomic DNA from:

  • 1-2 mm mouse ear clips
  • 3-5 mg tissue


If you wish to isolate genomic DNA from larger amounts of tissue or from mouse tail tips, see Isolating Genomic DNA Using the Mini Tissue Kit.

Materials Needed

Have the following materials on hand before beginning:

  • Tissue sample(s) (see above)
  • MagnaRack™ (Catalog no. CS15000) or other magnetic separation rack
  • Sterile 1.5 ml microcentrifuge tubes
  • Vortex mixer
  • Sterile pipette tips (20 µl, 200 µl, and 1 ml)
  • Water bath


Components Supplied with the Kit

  • ChargeSwitch® Lysis Buffer (L15)
  • Proteinase K
  • RNase A
  • ChargeSwitch® Magnetic Beads
  • ChargeSwitch® Purification Buffer (N5)
  • ChargeSwitch® Wash Buffer (W12)
  • ChargeSwitch® Elution Buffer (E5) or TE Buffer (not supplied; 10 mM Tris-HCl, 1 mM EDTA, pH 8.5)


Before Starting

Perform the following before beginning:

  • Set a water bath at 55° C.
  • Prepare Lysis Mix: For each sample, mix 1 ml of ChargeSwitch® Lysis Buffer (L15) and 10 µl of Proteinase K to prepare the Lysis Mix. When isolating DNA from multiple samples, scale up the volume of reagents used and prepare a master Lysis Mix.


Note:   The ChargeSwitch® Lysis Buffer may appear slightly cloudy. If cloudy, shake the bottle before use until the solution becomes clear.
 
Preparing the Tissue Lysate

Follow the procedure below to prepare a lysate from the tissue sample.

 

  1. Place the tissue sample into a sterile microcentrifuge tube.

  2. Add 1 ml of Lysis Mix (see above) to the tube. Ensure that the tissue is completely immersed in the Lysis Buffer.

  3. Vortex for 10-15 seconds to mix.

  4. Incubate the sample overnight at 55° C until lysis is complete.
     
    Note:   The length of the incubation step can be shortened to 1-2 hours by vortexing the sample at least 4 times during this period.

  5. Add 5 µl of RNase A to the lysate. Pipet up and down gently 5 times or until a homogeneous solution is obtained.
     
    Important:   Use a 1 ml pipette tip set to 900 µl to mix the sample. Make sure that the tip is submerged, and pipet up and down gently to avoid forming bubbles as this may result in shearing of the DNA.

  6. Incubate at room temperature for 5 minutes.

  7. Proceed to Binding DNA.



Binding DNA

Follow the procedure below to bind the DNA to the ChargeSwitch® Magnetic Beads.

  1. Vortex the tube containing the ChargeSwitch® Magnetic Beads to fully resuspend and evenly distribute the beads in the storage buffer. Make sure that all of the solution containing the beads is at the bottom of the tube.

  2. Add 200 µl of ChargeSwitch® Purification Buffer (N5) to the digested tissue sample and pipet up and down gently twice to mix. 

    Note:   Adding the ChargeSwitch® Purification Buffer lowers the pH of the sample, and optimizes the binding conditions.

  3. Add 40 µl of ChargeSwitch® Magnetic Beads (from Step 1) to the sample and pipet up and down gently 5 times to mix.

  4. Incubate at room temperature for 1 minute to allow the DNA to bind to the ChargeSwitch® Magnetic Beads.

  5. Place the sample in the MagnaRack™ for 1 minute or until the beads have formed a tight pellet.

  6. Without removing the tube from the MagnaRack™, carefully remove the supernatant and discard. Take care not to disturb the pellet of beads by angling the pipette such that the tip is pointed away from the pellet (see figure below).


  7. Proceed immediately to Washing DNA



Washing DNA

  1. Remove the tube containing the pelleted magnetic beads from the MagnaRack™.  There should be no supernatant in the tube.

  2. Add 1 ml of ChargeSwitch® Wash Buffer (W12) to the tube and pipet up and down gently twice to resuspend the magnetic beads.
     
    Important:   Use a 1 ml pipette tip set to 900 µl to mix the sample. Make sure that the tip is submerged, and pipet up and down gently to avoid forming bubbles.

  3. Place the sample in the MagnaRack™ for 1 minute or until the beads have formed a tight pellet.

  4. Without removing the tube from the MagnaRack™, carefully remove the supernatant and discard. Take care not to disturb the pellet of beads by angling the pipette such that the tip is pointed away from the pellet.

  5. Repeat Steps 1-4.

  6. Proceed to Eluting DNA.


 
Eluting DNA

  1. Remove the tube containing the pelleted magnetic beads from the MagnaRack™ (Step 5). There should be no supernatant in the tube.
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  2. Add 150 µl of ChargeSwitch® Elution Buffer (E5) (or TE Buffer, pH 8.5) to the tube and pipet up and down gently 10 times to resuspend the magnetic beads.

    Important:  Do not use water for elution. The DNA will not elute due to the poor buffering capacity of water.

  3. Incubate at room temperature for 5 minutes.
     
    Tip:   For maximum yield, mix the suspension of beads (by pipetting up and down gently) half way through the incubation. Incubating the sample at 55° C may also improve yield.

  4. Place the sample in the MagnaRack™ for 1 minute or until the beads have formed a tight pellet.

  5. Without removing the tube from the MagnaRack™, carefully remove the supernatant containing the DNA to a sterile microcentrifuge tube. Take care not to disturb the pellet of beads by angling the pipette such that the tip is pointed away from the pellet

    Note:  If the eluate containing the DNA is discolored, repeat Steps 5-6.

  6. Discard the used magnetic beads. Do not reuse the beads.


 
Storing DNA

  • Store the purified DNA at -20° C or use immediately for the desired downstream application.
  • Avoid repeatedly freezing and thawing DNA. Store the purified DNA at 4°C for short-term use or aliquot the DNA and store at -20°C for long-term storage.


Quantitating DNA Yield

You may estimate the yield of purified genomic DNA by checking the UV absorbance at 260 nm or using one of the Quant-iT™ DNA Assay Kits.
 
UV Absorbance

 

  1. Measure the A260 of the solution using a spectrophoto-meter blanked against 10 mM Tris-HCl, pH 8.5.

  2. Calculate the amount of DNA using the formula:
    DNA (µg) = A260 US 50 µg/(A260 x 1 ml) x dil’n factor x total sample volume (ml)
    For DNA, A260= 1 for a 50 µg/ml solution measured in a cuvette with an optical path length of 1 cm.


 
Quant-iT™ DNA Assay Kits

The Quant-iT™ DNA Assay Kits provide a rapid, sensitive, and accurate method for dsDNA quantitation with minimal interference from RNA, protein, ssDNA (primers), or other common contaminants that affect UV absorbance. Each kit contains a state-of-the-art quantitation reagent, pre-diluted standards for a standard curve, and a pre-made buffer to allow fluorescence-based DNA quantitation. For more information, see www.invitrogen.com or call Technical Service

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Troubleshooting

Introduction

Refer to the table below to troubleshoot problems that you may encounter when purifying genomic DNA with the kit.

Problem
Cause
Solution
Low DNA yield
Incomplete lysis
  • Decrease the amount of starting material used.
  • Be sure to add Proteinase K during lysis.
  • Make sure that the tissue is completely immersed in the Lysis Buffer.
  • Increase the length of incubation at 55°C.
  • For mini quantities of tissue, homogenize tissue before lysis.
 
Poor quality of starting material
Be sure to use fresh sample and process immediately after collection or freeze the sample at -80°C or in liquid nitrogen. The yield and quality of DNA isolated depends on the type and age of the starting material.
 
Insufficient amount of ChargeSwitch® Magnetic Beads added
Vortex the tube containing the ChargeSwitch® Magnetic Beads to fully resuspend the beads in solution before adding them to your sample.
 
Pellet of beads disturbed or lost during binding or washing steps
  • Keep the sample in the MagnaRack when removing supernatant during the binding or washing steps.
  • Remove the supernatant without disturbing the pellet of beads by angling the pipette tip away from the pellet.
Low DNA yield, continued
Incorrect elution conditions
  • After adding ChargeSwitch® Elution Buffer (E5) to the sample, pipet up and down to resuspend the magnetic beads before incubation.
  • Incubate the sample at 55°C to improve the yield.
  • Do not use water to elute DNA. Use Elution Buffer (E5) or TE, pH 8.5.
 
Incomplete dissociation of DNA from the ChargeSwitch® Magnetic Beads
  • Perform additional mixing of the suspension of beads (by pipetting up and down).
  • Elute DNA at 65° C.
No DNA recovered
Water used for elution
Do not use water for elution. The elution buffer must have a pH = 8.5-9.0 or the DNA will remain bound to the ChargeSwitch® Magnetic Beads. Use ChargeSwitch® Elution Buffer (E5) or TE, pH 8.5.
 
ChargeSwitch® Magnetic Beads stored or handled improperly
  • Store beads at room temperature. Do not freeze the beads as they will become irreparably damaged.
  • Make sure that the beads are in solution at all times and do not become dried. Beads that have dried out are non-functional.
Eluate containing DNA is discolored
Magnetic pellet disturbed during elution
Repeat the elution step (Eluting DNA).
RNA contamination
Forgot to add RNase A
Perform RNase A digestion prior to binding the DNA to the magnetic beads.
DNA is sheared or degraded
Lysate mixed too vigorously or small pipette tips used during mixing
  • Use a 1 ml pipette tip set to 900 µl to mix the sample.
  • Pipet up and down gently to mix.
 
Bubbles formed during mixing steps
Make sure that the pipette tip is submerged in the solution during mixing.
 
DNA repeatedly frozen and thawed
Aliquot DNA and store at 4°C or -20°C. Avoid repeated freezing and thawing.
 
DNA contaminated with DNases
Maintain a sterile environment while working (i.e. wear gloves and use DNase-free reagents).
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