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Biomiga

Plasmid Maxi Kit, 2 Preps, Biomiga


List price: $30.00  

$27.00

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Biomiga
PD1511-00
In stock
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The key to this kit is our proprietary DNA binding systems that allow the high efficient binding of DNA to our ezBindTM matrix while proteins and other impurities are removed by wash buffer. Nucleic acids are easily eluted with sterile water or Elution Buffer. Unlike other kits in the markets, our patented plasmid purification kit has no chaotropic salts in the buffer. The purified DNA is guanidine/anion exchange resin residues free.

This kit is designed for fast and efficient purification of plasmid DNA from 100 to 250 mL of E. coli culture. The maxi column has a plasmid DNA binding capacity of 1 mg.

The purified plasmid DNA is ready for downstream applications such as transfection of robust cells such as HEK293, restriction mapping, library screening, sequencing, as well as gene therapy and genetic vaccinations.

 

Citations

Murine Xenograft Model for Human Uterine Fibroids: An In Vivo Imaging Approach.  Reproductive Sciences, 2009, 16(9), 827-842

Characterization of monoclonal antibodies against goat interleukin-18 and their application in the measurement of goat interleukin-18 in LPS-stimulated peripheral blood mononuclear cells by sandwich ELISA. Veterinary Immunology and Immunopathology, Volume 138, Issue 3, 2010, 235-238

Platelet-Derived Growth Factor C Is Upregulated in Human Uterine Fibroids and Regulates Uterine Smooth Muscle Cell Growth1. Biology of Reproduction, 2009, vol. 81 no. 4749-758

Cloning, characterization and tissue distribution of a pi-class glutathione S-transferase from clam (Venerupis philippinarum): Response to benzo[?]pyrene exposure. Comparative Biochemistry and Physiology, Part C: Toxicology & Pharmacology , 2010,Volume 152, Issue 2, August 2010, Pages 160-166

 

Important Notes

Plasmid Copy Numbers: The yield of plasmid DNA depends on the origin of the replication and the size of the plasmid. The protocols are optimized for high copy number plasmid purification. For low copy number plasmids, both the culture volume and the buffer volume need to be scaled up 2 to 3 times. Reference Table 1 for the commonly used plasmids,

Table 1 Commonly used plasmids.

Plasmid

Origin

Copy Numbers

Expected Yield(µg per  200 mL)

PSC101

pSC101

5

12

pACYC

P15A

10-12

25-40

pSuperCos

pMB1

10-20

30-50

PBR322

pMB1

15-20

35-50

pGEMR

Muted pMB1

300-400

350-450

pBluescriptR

ColE1

300-500

450-600

PUC

Muted pMB1

500-700

700-1,000

Host Strains:The strains used for propagating plasmid have significant influence on yield. Host strains such as Top 10 and DH5a yield high-quality plasmid DNA. endA+ strains such as JM101,  JM110, HB101, TG1 and their derivatives, normally have low plasmid yield due to either endogenous endonucleases or high carbohydrates released during lysis. We recommend transform plasmid to an endA- strain if the yield is not satisfactory.  For purifying plasmid DNA from endA+ strains (Table 2), we recommend use product PD1713.  

Table2 endA+ strains of E. Coli.

EndA-Strains of E. Coli

DH5α

DH1

DH21

JM106

JM109

SK2267

SRB

XLO

TOP10

DH10B

JM103

JM107

SK1590

MM294

Stbl2TM

XL1-Blue

BJ5182

DH20

JM105

JM108

SK1592

Select96TM

Stbl4TM

XL10-Gold

 

EndA+Strains of E. Coli

C600

JM110

RR1

ABLE® C

CJ236

KW251

P2392

BL21(DE3)

HB101

TG1

TB1

ABLE® K

DH12STM

LE392

PR700

BL21(DE3)pLysS

JM101

JM83

TKB1

HMS174

ES1301

M1061

Q358

BMH 71-18

All NM  strains

All Y strains

Optimal Cell Mass (OD600 x mL of Culture):This procedure is designed for isolating plasmid grown in standard LB medium (Luria Bertani) for 12 -16 hours to a density of OD600 2.0 to 3.0. If rich medium such as TB or 2xYT are used, make sure the cell density doesn't exceed 3.0 (OD600). A high ratio of biomass over lysis buffers result in low DNA yield and purity. The maxi column has an optimal biomass of 450-550. For example, if the OD600 is 2.5, the optimal culture volume should be 200 mL.

Culture Volume: Use a flask or tube 4 times larger in volume than the culture medium to secure optimal condition for bacteria growth. Don't exceed the maximum culture volume suggested in the protocol. Incomplete lysis due to over amount of bacterial culture results in lower yield and less purity.

 

Storage and Stability

Buffer A1 should be stored at 4°C once RNase A is added. All other materials can be stored at room temperature (22-25°C). The Guaranteed shelf life is 12 months from the date of purchase.

 

Before Starting

Prepare all components and get all necessary materials ready by examining this instruction booklet and become familiar with each step.

 

Important

  • RNase A: It is stable for more than half a year when stored at room temperature. Spin down the RNase A vial briefly. Add the RNase A solution to Buffer A1 and mix well before use, and then store at 4oC.
  • Buffer B1 precipitates below room temperature. It is critical to warm up the buffer at 50oC to dissolve the precipitates before use.
  • Incubating Buffer C1 at 4 oC before experiment will decrease the floating precipitates.
  • Keep the cap tightly closed for Buffer B1 after use.
  • Make sure the availability of centrifuge and vacuum manifold, especially, after mixing the lysate with ethanol, the sample needs to be processed immediately either by centrifugation or vacuum.
  • Carry out all centrifugations at room temperature.

 

Materials supplied by users

  • 70% ethanol and 100% ethanol
  • High speed centrifuge
  • 30 mL high speed centrifuge tubes
  • 50 mL tubes

 

Kit contents

Catalog#

PD1511-00

PD1511-01

PD1511-02

Preps

2

10

25

ezBindTM Columns

2

10

25

Buffer A1

22 mL

110 mL

270 mL

Buffer B1

22 mL

110 mL

270 mL

Buffer C1

27 mL

135 mL

330 mL

RNase A(20 mg/mL)

2.2 mg(110 µL)

11 mg(550 µL)

27 mg(1.35 µL)

Elution Buffer

6 mL

30 mL

60 mL

User Manual

1

1

1

 

Safety Information

  • Buffer C1 contains acidic acid, wear gloves and protective eyewear when handling.
  • Buffer C1 contains chaotropic salts, which may form reactive compounds when combines with bleach. Do not add bleach or acidic solutions directly to the preparation waste.

 

Operating Protocol

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