MspJI

Catalog # Concentration Size List Price Quantity Your Price
R0661L 5000 units/ml 1000 units $767.00
$690.30
R0661S 5000 units/ml 200 units $186.00
$167.40
Catalog # Size List Price Your Price
R0661L 1000 units $767.00
$690.30
R0661S 200 units $186.00
$167.40
Catalog #
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*On-line ordering is for Canadian customers only. Web pricing is applicable only to orders placed online at www.neb.ca
  • 100% activity in rCutSmart Buffer (over 210 enzymes are available in the same buffer) allowing for easier double digests
  • Specificity to epigenetically-relevant DNA modifications (5-mC and 5-hmC)
  • Restriction Enzyme Cut Site: CNNR(9/13)
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MspJI, an EpiMark®, validated product is a modification-dependent endonuclease that recognizes mCNNR sites and generates a double-stranded DNA break on the 3´ side of the modified cytosine at N9/N13. The recognized cytosine modifications include C5-methylation (5-mC) and C5-hydroxymethylation (5-hmC) (1).

This enzyme is provided with an Enzyme Activator Solution which may be used for efficient digestion by MspJI.

The most common epigenetic modifications found in eukaryotic organisms are methylation marks at CpG or CHG sites. A subset of these modified sites are recognized and cleaved by MspJI.

At fully methylated CpG sites:
5´ . . . Y N mC G N R . . . 3´
3´ . . . R N G mC N Y . . . 5´

or CHG sites:
5´ . . . Y mC H G R . . . 3´
3´ . . . R G D mC Y . . . 5´

R = A or G
Y = C or T
H = A or C or T (not G)
D = A or G or T (not C) 

MspJI recognizes each hemi-methylated site individually and cleaves bidirectionally to generate 32-base or 31-base fragments, respectively. These fragments contain the central methylated site and have 4-base 5´ overhangs at each end. MspJI does not cleave unmodified DNA.
Product Source
An E. coli strain that carries the synthetic MspJI gene from Mycobacterium species JLS.
Reagents Supplied

The following reagents are supplied with this product:

NEB # Component Name Component # Stored at (°C) Amount Concentration
  MspJI R0661SVIAL -20 1 x 0.04 ml 5,000 units/ml
  rCutSmart™ Buffer B6004SVIAL -20 1 x 1.25 ml 10 X
  Enzyme Activator Solution S0538SVIAL -20 1 x 0.1 ml 15 µM
  MspJI R0661LVIAL -20 1 x 0.2 ml 5,000 units/ml
  rCutSmart™ Buffer B6004SVIAL -20 1 x 1.25 ml 10 X
  Enzyme Activator Solution S0538LVIAL -20 1 x 0.5 ml 15 µM
MspJI | New England Biolabs

MspJI
neb31 cloned at NEB recombinant dil_B 37 65 Heat Epi

We are excited to announce that all reaction buffers are now BSA-free. NEB began switching our BSA-containing reaction buffers in April 2021 to buffers containing Recombinant Albumin (rAlbumin) for restriction enzymes and some DNA modifying enzymes. Find more details at www.neb.com/BSA-free.

NEB restriction endonuclease that recognizes the sequence CNNRNNNNNNNNN^NNNN_
Isoschizomers | Single Letter Code | Pronunciation:
  • 100% activity in rCutSmart Buffer (over 210 enzymes are available in the same buffer) allowing for easier double digests
  • Specificity to epigenetically-relevant DNA modifications (5-mC and 5-hmC)
  • Restriction Enzyme Cut Site: CNNR(9/13)

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Catalog https://www.neb.com/en/# Concentration Size
R0661S 5,000 units/ml 200 units
R0661L 5,000 units/ml 1,000 units
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Materials Sold Separately
Notes
  • This enzyme has been used for epigenetic analysis in which target DNA containing CpG sites methylated in both strands is cleaved by MspJI to generate 32 bp fragments containing the methylated CpG sites. The isolated 32 bp fragments can be sequenced to reveal 5-mC modification sites (Cohen-Karni et al., (2011) PNAS 108: 11040-11045).
  • Use of excess enzyme inhibits cleavage. Optimization of the amount of enzyme needed for complete digestion may be required for each substrate DNA.
  • Star activity, including digestion of non-methylated DNA substrates, may result from non-optimal reaction conditions such as extended digestion time, high enzyme or activator concentration or a glycerol concentration of > 5%. Optimization of the amount of enzyme needed to achieve efficient specific cutting, while avoiding star activity, may be required for each substrate DNA.
  • Optimal specificity of cleavage at 5-mC sites can be achieved by keeping the molar ratio of MspJI to 5-mC target sites between 0.1:1 to 1:1 in the presence of 1X Enzyme Activator Solution and digesting for up to 60 minutes. (The molarity of MspJI is ~7.4 μM).
  • Not sensitive to CpG, dcm, or dam methylation.
References
  • Zheng, Y. et al. (2010). Nucl. Acids Res. doi:10, 1093/nar/gkq327.
  • U.S. Publication No. 2010-0167942 Unpublished observation
  • Cohen-Karni D et al. (2011). The MspJI family of modification dependent restriction endonucleases for epigenetic studies.. Proc. Natl. Acad. Sci. U.S.A.. Jul 5;108(27):, 11040-5.
Additional Citations
  • Cohen-Karni, D, et al. (2011) The MspJI family of modification-dependent restriction endonucleases for epigenetic studies Proc Natl Acad Sci U S APubMedID: 21690366, DOI: 10.1073/pnas.1018448108
Publications
  • Horton, J.R., Mabuchi, M., Cohen-Karni, D., Zhang, X., Griggs, R., Samaranayake, M., Roberts, R.J., Zheng, Y. and Cheng, X. (2012). Stucture and cleavage activity of the tetrameric MspJI DNA modification-dependent restriction endonuclease. Nucleic Acids Res. 40(19),PubMedID: 22848107
Quality Control Assay
Quality Control tests are performed on each new lot of NEB product to meet the specifications designated for it. Specifications and individual lot data from the tests that are performed for this particular product can be found and downloaded on the Product Specification Sheet, Certificate of Analysis, data card or product manual. Further information regarding NEB product quality can be found here.
Specifications
The Specification sheet is a document that includes the storage temperature, shelf life and the specifications designated for the product. The following file naming structure is used to name these document files: [Product Number]_[Size]_[Version]
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