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ProCipitate, substitute to phenol / chloroform

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ProCipitate, substitute to phenol / chloroform
Protein removal/DNA enrichment & isolation reagent 
 
무해한 단백질 제거 시약으로, 핵산 정제에 있어서 phenol/chloroform의 대체품으로 사용할 수 있습니다. 음전하를 띤 고분자 전해질을 기반으로 하고 있으며, 단백질 용액에 첨가하면 전하가 중화되고 단백질이 불용화됩니다. 핵산에 결합하지 않기 때문에 높은 회수율, 고 품질의 DNA 및 RNA를 정제할 수 있습니다. 
 
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Agarose gel electrophoresis and Southern blot analysis comparing genomic DNA from yeast purified by phenol/chloroform and by ProCipitate™.
 
A.
Lanes 1-4 are isolated by traditional phenol/ chloroform methods.
Lanes 5-8 were purified using non-hazardous ProCipitate™
Lanes 1 & 5 are undigested.
The other lanes were digested with restriction enzymes as follows:
(BAM HI – lanes 2 & 4),(Eco RI – lanes 3 & 7), (Hind III – lanes 4 & 8)
B.
Southern Blot. The DNA was transferred and hybridized to a labeled probe and exposed to film for 3 hours.
Lanes 1-8 correspond to A. 
 
ProCipitate™ 
  • Non-hazardous substitute to phenol/chloroform
  • Removes only the contaminants & leaves DNA alone
  • Improves yield of DNA over alternative bind and elute systems
  • Adaptable to any sample size, and can be automated
  • Key component of the ProPrep™ line of application specific kits 
ProCipitate™ is a unique protein removal reagent based upon patented elastomeric polyelectrolytes. The polymer chains of ProCipitate™ are initially extended in a high energy state due to an overall net
negative charge. When introduced to protein solutions, the charges are neutralized and the polymer chains collapse to a more favorable energy state; DNA and RNA remain unreacted. ProCipitate™ is 
non-hazardous and can replace phenol/chloroform with the additional benefits of solid-phase suspensions: adaptability to filtration and automation. It is routinely used for plasmids, cosmids, BACs, and
genomic DNA, as well as RNA. ProCipitate™ can also be used to remove Proteinase K and other enzymes. ProCipitate™ provides high quality DNA suitable for automated sequencing, southern blotting, 
and restriction digestion. ProCipitate™ is available as a suspension reagent and in ProPrep™ kits for specific applications and high-throughput 96 well filter formats. 
 
Performance Characteristics 
Protein
ProCipitate : Sample
Removal
BSA, PBS @ 30 mg/ml
1 : 1
> 99%
BSA, 1%SDS @ 30 mg/ml
1 : 1
> 99%
BSA, 3M GuSCN @ 30 mg/ml
1 : 1
> 95%
Human Serum
1 : 1
> 90%
Human Serum, 1% Surfactant
1 : 1
> 95%
 
Nucleic Acid Recovery
ProCipitate : Sample
Removal
Calf Thymus DNA, A260 = 1.00
1 : 1
> 95%
Total RNA, A260 = 1.00
1 : 1
> 99%
 
  
 
References ;
  1. U.S. Patent Numbers 5,294,681, 5,453,493 and other patents pending.
  2. U.S. Patent Number 5,538,870, Method for Preparing Nucleic Acids For Analysis And Kits Useful Therefore.
  3. Transgenic labeling of hair cells in the zebrafish acousticolateralis system Brian M. McDermott Jr Gene Expression Patterns Volume 10, Issues 2-3, February-March 2010, Pages 113-118
  4. Formation of Deoxyguanosine Cross-Links from Calf Thymus DNA Treated with Acrolein and 4-Hydroxy-2-nonenal. Ivan D. Kozekov, Robert J. Turesky, Guillermo R. Alas, Constance M. Harris, Thomas M. Harris, Carmelo J. Rizzo Chemical Research in Toxicology 2010 23 (11), 1701-1713
  5. Genome-wide sequence and functional analysis of early replicating DNA in normal human fibroblastsStephanie M Cohen, Terrence S Furey, Norman A Doggett, and David G Kaufman BMC Genomics. 2006; 7: 301. Published online 2006 November 29. doi: 10.1186/1471-2164-7-301.
  6. Dr. Domon, National Agricultural Research Center for Kyushu Okinawa Region, Japan, Extraction of Rush DNA, unpublished personal correspondence, 2004.
  7. Krupey, J., et al, 100,000+ PCRs Possible from 10 ml Blood, poster Biotechniques Symposium, 2003.
  8.  
Ordering informations ; 
1. P0050-30   : ProCipitate™(30ml)
2. P0050-100 :  ProCipitate™(100ml)
 
 

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