Human MMP24 knockout HeLa cell line
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MMP24 KO cell line available to order. KO validated by. Free of charge wild type control provided. Knockout achieved by using CRISPR/Cas9, 25 bp deletion in exon 2 and 8 bp deletion in exon 2.
View Alternative Names
MMP24_HUMAN, MT-MMP 5, MT5-MMP, Matrix metallopeptidase 24, Matrix metallopeptidase 24 (membrane inserted), Membrane-type matrix metalloproteinase 5, Membrane-type-5 matrix metalloproteinase, Processed matrix metalloproteinase-24
- Sanger seq
Unknown
Sanger Sequencing - Human MMP24 knockout HeLa cell line (AB265211)
Allele-1 : 25 bp deletion in exon 2.
- Sanger seq
Unknown
Sanger Sequencing - Human MMP24 knockout HeLa cell line (AB265211)
Allele-2 : 8 bp deletion in exon 2.
Product details
Recommended control: Human wild-type HeLa cell line (ab255928). Please note a wild-type cell line is not automatically included with a knockout cell line order, if required please add recommended wild-type cell line at no additional cost using the code WILDTYPE-TMTK1.
We will provide viable cells that proliferate on revival.
This product is subject to limited use licenses from The Broad Institute and ERS Genomics Limited, and is developed with patented technology. For full details of the limited use licenses and relevant patents please refer to our limited use license and patent pages.
What's included?
Properties and storage information
Gene name
Gene editing type
Gene editing method
Knockout validation
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Handling procedures
Initial handling guidelines
Upon arrival, the vial should be stored in liquid nitrogen vapor phase and not at -80°C. Storage at -80°C may result in loss of viability.
1. Thaw the vial in 37°C water bath for approximately 1-2 minutes.
2. Transfer the cell suspension (0.8 mL) to a 15 mL/50 mL conical sterile polypropylene centrifuge tube containing 8.4 mL pre-warmed culture medium, wash vial with an additional 0.8 mL culture medium (total volume 10 mL) to collect remaining cells, and centrifuge at 201 x g (rcf) for 5 minutes at room temperature. 10 mL represents minimum recommended dilution. 20 mL represents maximum recommended dilution.
3. Resuspend the cell pellet in 5 mL pre-warmed culture medium and count using a haemocytometer or alternative cell counting method seed all remaining cells into a T25.
4. Incubate the culture at 37°C incubator with 5% CO2. Check the culture one day after revival and continue to check until 80% confluent. Media change can be given if needed.
5. Once confluent passage into an appropriate flask at a density of 2x104 cells/cm2. Seeding density is given as a guide only and should be scaled to align with individual lab schedules. Cultures should be monitored daily.
Subculture guidelines
- All seeding densities should be based on cell counts gained by established methods.
- A guide seeding density of 2x104 cells/cm2 is recommended.
- Cells should be passaged when they have achieved 80-90% confluence.
Culture medium
DMEM (High Glucose) + 10% FBS
Cryopreservation medium
Cell Freezing Medium-DMSO Serum free media, contains 8.7% DMSO in MEM supplemented with methyl cellulose.
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The enzyme is involved in the modulation of synaptic connections and neural plasticity. MMP24 functions as part of a complex which includes pro-protein convertases that activate the enzyme from its pro-form. These activities highlight its contribution to the regulation of neural networks. MMP24's interaction with neuronal substrates and their subsequent processing is vital for maintaining normal neural architecture and response to recovery processes after injury.
Pathways
MMP24 holds a significant role in the extracellular matrix (ECM) remodeling pathway and is linked to the integrin signaling pathway. These pathways are important for cell adhesion migration and survival. In the ECM remodeling pathway MMP24 interacts with other metalloproteinases such as MMP2 and MMP9 highlighting its contribution to the dynamic remodeling processes. In the integrin signaling pathway its activity affects cell-matrix interactions emphasizing its importance in cellular communication and structural organization within tissues.
Quality control
STR analysis
D7S820, D5S818, TH01, D16S539, TPOX, CSF1PO, D13S317
Cell culture
Biosafety level
EU: 2 US: 2
Adherent/suspension
Adherent
Gender
Female
Target data
Complementary Products
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com