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444232 MMP-9, Dimer, Human Neutrophil

MMP-9, Dimer, Human Neutrophil MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

同义词: Matrix Metalloproteinase 9, Gelatinase B, 92 kDa type IV Collagenase

444232
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概述

Replacement Information

Products

产品目录编号包装 数量 / 包装
444232-5UGCN 塑胶安瓿;塑胶针药瓶 5 μg
Description
OverviewDimeric, native MMP-9 from stimulated human neutrophils. Enzyme should be activated just prior to use.
M.W. 222,000 (non-reducing SDS-PAGE). Note: 1 mU = 1 milliunit.
Catalogue Number444232
Brand Family Calbiochem®
SynonymsMatrix Metalloproteinase 9, Gelatinase B, 92 kDa type IV Collagenase
References
ReferencesOlson, M.W. et al. 2000. J. Biol. Chem. 275, 2661.
Kolkenbrock, H., et al. 1996. Biol. Chem. 377, 529.
Product Information
Unit of DefinitionOne unit is defined as the amount of enzyme that will hydrolyze 1.0 µmol 2,4-DNP-Pro-Gln-Gly-Ile-Ala-Gly-Gln-D-Arg-OH per min at 37°C pH 7.0.
EC number3.4.24.35
FormLiquid
FormulationIn 200 mM NaCl, 50 mM Tris-HCl, 5 mM CaCl₂, 1 µM ZnCl₂, 0.05% BRIJ® 35 Detergent, 0.05% NaN₃, pH 7.0.
Quality LevelMQ100
Applications
Biological Information
Purity≥90% by SDS-PAGE
SourcePrepared from stimulated neutrophils that have been shown by certified tests to be negative for HBsAg and for antibodies to HIV and HCV.
Specific Activity≥1000 mU/mg protein
Physicochemical Information
ContaminantsNo other MMP activity detectable
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Dry Ice Only
Toxicity Standard Handling
Storage ≤ -70°C
Avoid freeze/thaw Avoid freeze/thaw
Do not freeze Ok to freeze
Special InstructionsFollowing initial thaw, aliquot and freeze (-70°C).
Packaging Information
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
产品目录编号 GTIN
444232-5UGCN 04055977186390

Documentation

MMP-9, Dimer, Human Neutrophil MSDS

职位

物料安全数据表 (MSDS) 

MMP-9, Dimer, Human Neutrophil 分析证书

标题批号
444232

参考

参考信息概述
Olson, M.W. et al. 2000. J. Biol. Chem. 275, 2661.
Kolkenbrock, H., et al. 1996. Biol. Chem. 377, 529.
数据表

Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

Revision18-July-2007 RFH
SynonymsMatrix Metalloproteinase 9, Gelatinase B, 92 kDa type IV Collagenase
DescriptionDimeric, native MMP-9 from stimulated human neutrophils. Enzyme should be activated just prior to use.
FormLiquid
FormulationIn 200 mM NaCl, 50 mM Tris-HCl, 5 mM CaCl₂, 1 µM ZnCl₂, 0.05% BRIJ® 35 Detergent, 0.05% NaN₃, pH 7.0.
Recommended reaction conditions

Organomercurial Activation Protocol This protocol is provided only as a general guide. Researchers should standardize this assay for their own specific needs and should consult published literature. The following protocol is from Stricklin, et al., which describes the use of p-aminophenylmercuric acetate (APMA) to activate pro-MMP. This protocol is also adaptable to other types of organomercurals, such as p-(hydroxymercuric) benzoate (PHMB), phenylmercuric chloride (PMC), or mersalyl. 1. Prepare a 10-50 mM stock solution of APMA (or other organomercurial compound) in 0.1 M NaOH just prior to use. Although not absolutely necessary, the stock solution may be adjusted to pH 11 with 5 N HCl (see Marcy, A.I., et al.). 2. To initiate the activation mix the proenzyme solution with the APMA solution at a 10:1 volume ratio (MMP:APMA). If a higher concentration of APMA is desired, increase the concentration of the stock solution. Do not exceed the 10:1 ratio, as this could result in significant changes in pH. 3. Incubate the mixture at 37°C for 2-3 h. It is recommended that an analytical run be conducted first to determine the optimal incubation time. For example, a small-scale experiment with a fixed concentration of pro-MMP and organomercurial would be incubated as described above. Remove aliquots of the sample at various time points during the incubation. Stop the reaction by the addition of SDS-PAGE sample buffer (e.g., 10 µl 2X sample buffer to 10 µl aliquot) and heat the samples to 95°C. The progress of activation can be monitored qualitatively by analyzing the aliquots on a 12% SDS-PAGE gel. 4. The activated MMP can be used without removing the APMA from the mixture. Please refer to Marcy, A.I., et al. for removal of organomercurials by gel filtration.
SourcePrepared from stimulated neutrophils that have been shown by certified tests to be negative for HBsAg and for antibodies to HIV and HCV.
EC number3.4.24.35
Purity≥90% by SDS-PAGE
ContaminantsNo other MMP activity detectable
Specific activity≥1000 mU/mg protein
Unit definitionOne unit is defined as the amount of enzyme that will hydrolyze 1.0 µmol 2,4-DNP-Pro-Gln-Gly-Ile-Ala-Gly-Gln-D-Arg-OH per min at 37°C pH 7.0.
Storage Avoid freeze/thaw
≤ -70°C
Do Not Freeze Ok to freeze
Special InstructionsFollowing initial thaw, aliquot and freeze (-70°C).
Toxicity Standard Handling
ReferencesOlson, M.W. et al. 2000. J. Biol. Chem. 275, 2661.
Kolkenbrock, H., et al. 1996. Biol. Chem. 377, 529.