Anti-Matrix Metalloproteinase-24, Cytoplasmic antibody produced in rabbit (M6559) - Datasheet
ANTI-MATRIX METALLOPROTEINASE-24 (MMP-24,
MT5-MMP), CYTOPLASMIC DOMAIN
Developed in Rabbit, Affinity
thesis, pp. 94, 95 (2018).
10. Mouzannar, Raymond, "Higher order chromatin
degradation induced by hydrogen peroxide in glial
cells". West Virginia University, Ph.D. dissertation,
p. 24 (2001).
Di Cola, E. et al., Biomacromolecules, 9(11),
3216-3222 (2008).
6. Veluraja, K. et al., Biochem. Biophys. Res.
Comm., 406(94), 570-573 (2011).
7. Waldbrook, Matthew George, "In vivo efficacy
or
37 °C, 80-90% of initial activity is found after 24 hours.
The reconstituted product is stable for at least 3 hours
at 50 °C and for at least 24 hours at –20 °C.
References
1. Thelander, L., and
glucose-6-phosphate
0.4 U/ml glucose-6-phosphate dehydrogenase
3.3 mM magnesium chloride
0.2 mM diclofenac
100 mM Tris-HCl buffer, pH 7.5
The reaction was stopped with 50 µl of a 94%
acetonitrile
glucose-6-phosphate
0.4 U/ml glucose-6-phosphate dehydrogenase
3.3 mM magnesium chloride
0.2 mM diclofenac
100 mM Tris-HCl buffer, pH 7.5
The reaction was stopped with 100 µl of a 94%
acetonitrile
mM glucose-6-phosphate
0.4 U/ml glucose-6-phosphate dehydrogenase
3.3 mM magnesium chloride
0.1 mM 14C-lauric acid
100 mM Tris-HCl, pH 7.5
The reaction was stopped with 50 µl of 94%
Acetonitrile
glucose-6-phosphate
0.4 U/ml glucose-6-phosphate dehydrogenase
3.3 mM magnesium chloride
30 µM leukotriene B4
100 mM phosphate, pH 7.4
The reaction was stopped with 25 µl of
glucose-6-phosphate
0.4 U/ml glucose-6-phosphate dehydrogenase
3.3 mM magnesium chloride
0.2 mM diclofenac
100 mM Tris-HCl buffer, pH 7.5
The reaction was stopped with 100 µl of a 94%
acetonitrile
D., Methods
Enzymol., 57, 3-15 (1978).
6. Chappelle, E. W. et al., Methods Enzymol., 57,
65-72 (1978).
7. Karl, D. M., Methods Enzymol., 57, 85-94 (1978).
8. Afrin, Farzana, "Investigation
and Chamberlin, M. J., Nucleic
Acids Res., 24 (14), 2774-2781 (1996).
5. Newton, C. R., (Ed.) PCR: Essential Data, John
Wiley & Sons, New York (1995).
6. Sambrook, J., et al. Molecular Cloning:
mM glucose-6-phosphate
0.4 U/ml glucose-6-phosphate dehydrogenase
3.3 mM magnesium chloride
30 µM leukotriene B4
100 mM phosphate, pH 7.4
The reaction was stopped with 25 µl of 94%
acetonitrile