BfmI (SfcI)

Kód produktu: ER1161 Kód výrobce: ER1161 Kód dodavatele: {3E11B824-B959-44B3-BF5A-97BEE014FBE0} Výrobce: Life Technologies Czech Republic s.r.o.

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Detailní popis

Thermo Scientific conventional restriction endonucleases are a large collection of high quality restriction enzymes, optimized to work in one of the buffers of the Five Buffer System. In addition, the universal Tango buffer is provided for convenience in double digestions. All of the enzymes exhibit 100% activity in the recommended buffer and reaction conditions. To ensure consistent performance, Thermo Scientific restriction enzyme reaction buffers contain premixed BSA, which enhances the stability of many enzymes and binds contaminants that may be present in DNA preparations.

Highlights

Superior quality – stringent quality control and industry leading manufacturing process
Convenient color-coded Five Buffer System
Includes universal Tango buffer for double-digestions
BSA premixed in reaction buffers
Wide selection of restriction endonuclease specificities

Applications

Molecular cloning
Restriction site mapping
Genotyping
Southern Blot
Restriction fragment length polymorphism (RFLP)
SNP

Note

For methylation sensitivity refer to product specifications.

Compatible Ends	`C↓TGCAG` - Alw44I.
Conditions for 100% Activity	1X Buffer Tango: 33 mM Tris-acetate (pH 7.9 at 37°C), 10 mM Mg-acetate, 66 mM K-acetate, and 0.1 mg/mL BSA Incubate at 37°C
Double Digestion	Perform double digestion using DoubleDigest.
Hazardous	No
Isoschizomers	Search for commercial isoschizomers using REsearch.
Note	Low salt, high glycerol (> 5%) concentrations, pH > 8.0 or a large excess of enzyme may result in star activity.
Storage Buffer	BfmI is supplied in: 10 mM Tris-HCl (pH 7.4 at 25°C), 100 mM KCl, 1 mM DTT, 1 mM EDTA, 0.2 mg/mL BSA, and 50% (v/v) glycerol.
Storage Condition	-20 C

Reaction conditions

Recommended buffer for 100% activity	Optimal temperature	Enzyme activity in Thermo Scientific buffers, %						Tango buffer for double digestion
Recommended buffer for 100% activity	Optimal temperature	B (blue) 1X	G (green) 1X	O (orange) 1X	R (red) 1X	Tango (yellow) 1X / 2X		Tango buffer for double digestion
Tango	37°C	0-20	50-100	0-20	0-20	100	20-50	1X or 2X

Methylation Effects

Dam: never overlaps - no effect.
Dcm: never overlaps - no effect.
CpG: never overlaps - no effect.
EcoKI: never overlaps - no effect.
EcoBI: never overlaps - no effect.

Cleavage efficiency close to the termini of PCR fragments

bp from the recognition site to fragment end
1	2	3	4	5
50-100

Number of recognition sites in DNA molecules

Lambda	ΦX174	M13mp18/19	pBR322	puc18/19	pUC57
38	6	7	4	4	4
pTZ19R/U	pTZ57R	pBluescriptIIKS(-/+)	pBluescriptIISK(-/+)	pACYC177	pACYC184
6	6	6	6	1	1

New sites generated by ligation

Newly generated recognition sites resulting from ligation of protruding compatible DNA ends

Recognition Sequence	Second Enzyme	Enzymes recognizing newly generated recognition sequence
`C^TGCAG`	Alw44I (ApaLI)/FastDigest ApaLI (Alw44I) (`G^TGCAC`)	HpyCH4V

Newly generated recognition sites resulting from fill-in of 5'-overhang and self-ligation

Recognition Sequence	Newly generated sequence after reaction	Enzymes that cleave the newly generated sequence
`C^TRYAG`	`CTRYATRYAG`	FaiI
`C^TACAG`	`CTACATACAG`	FaiI
`C^TATAG`	`CTATATATAG`	[FaiI]
`C^TGCAG`	`CTGCATGCAG`	Cac8I CviAII FaiI FatI Hin1II (NlaIII)/FastDigest NlaIII (Hin1II) [HpyCH4V] PaeI (SphI)/FastDigest SphI (PaeI) XceI (NspI)/FastDigest NspI (XceI)
`C^TGTAG`	`CTGTATGTAG`	FaiI

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