Restriction Home.
SNP detection with mutagenic primers
Input sequence will be searched to find changes in one nucleotide near the location of the SNP,
so that mutagenic primers may be easily designed.
Example
DNA sequence (number, spaces and line feeds will be ignored)
Tidy Up
Reverse
Complement
SNP is located at position
, the alternative nucleotide to be detected is
,
and one mismatch is generated at positions -6 to -2 and +2 to +6
Minimum recognition size for each restriction enzyme
4
5
6
7
8
Type of restriction enzyme
All
Blunt ends
Overhang end
Commercial source
All
Amersham Pharmacia Biotech
Minotech Biotechnology
Stratagene
Fermentas AB
Qbiogene
American Allied Biochemical, Inc.
SibEnzyme Ltd.\n
Nippon Gene Co., Ltd.
Takara Shuzo Co. Ltd.
Roche Applied Science
New England Biolabs
Toyobo Biochemicals
Megabase Research Products
CHIMERx
Promega Corporation
Sigma Chemical Corporation
Bangalore Genei
MRC-Holland
EURx Ltd.
Only restriction enzymes with known bases (no N,R,Y...)
Include Type IIb restriction enzymes (Two cleaves per recognition sequence)
Include Type IIs restriction enzymes (Non-palindromic and cleavage outside of the recognition site)
DNA sequences can be pasted as shown or just as a one line string (number, spaces and line feeds will be ignored)
Upload a reference SNP ID from NCBI (p.e.: rs1000000)
:
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