HAPLN3 KO cell line available to order. Free of charge wild type control provided. Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon 3 and 4 bp deletion in exon 3.
Images
Key facts
- Cell type
- A549
- Species or organism
- Human
- Tissue
- Lung
- Form
- Liquid
- Knockout validation
- Sanger Sequencing
- Mutation description
- Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon 3 and 4 bp deletion in exon 3
Alternative names
EXLD1, Extracellular link domain containing, 1, HAPLN3, HPLN3_HUMAN, HsT19883, Hyaluronan and proteoglycan link protein 3
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HAPLN3 KO cell line available to order. Free of charge wild type control provided. Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon 3 and 4 bp deletion in exon 3.
Key facts
- Cell type
- A549
- Species or organism
- Human
- Tissue
- Lung
- Form
- Liquid
- Knockout validation
- Sanger Sequencing
- Mutation description
- Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon 3 and 4 bp deletion in exon 3
- Disease
- Carcinoma
- Concentration
Properties
- Gene name
- HAPLN3
- Gene editing type
- Knockout
- Gene editing method
- CRISPR technology
- Knockout validation
- Sanger Sequencing
Quality control
- STR analysis
- CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX
Cell culture
- Biosafety level
- EU: 1 US: 1
- Adherent/suspension
- Adherent
- Gender
- Male
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.
- Do not allow the cell density to exceed 7x104 cells/cm2.
- Culture medium
- F-12K + 10% FBS
- Cryopreservation medium
- Cell Freezing Medium-DMSO Serum free media, contains 8.7% DMSO in MEM supplemented with methyl cellulose.
Storage
- Shipped at conditions
- Dry Ice
- Appropriate short-term storage conditions
- -196°C
- Appropriate long-term storage conditions
- -196°C
Notes
We will provide viable cells that proliferate on revival.
This product is subject to limited use licenses from The Broad Institute, ERS Genomics Limited and Sigma-Aldrich Co. LLC, and is developed with patented technology. For full details of the licenses and patents please refer to our limited use license and patent pages.
Supplementary info
- This supplementary information is collated from multiple sources and compiled automatically.
- Activity summary
HAPLN3 also known as hyaluronan and proteoglycan link protein 3 mechanically acts to stabilize the extracellular matrix structure by binding hyaluronic acid and proteoglycans. This protein has a mass of about 38 kDa. HAPLN3 is notably expressed in tissues like cartilage and brain contributing to its functional roles in these areas. Among its alternate names cartilage link protein 3 is recognized underlining its connection with connective tissues.
- Biological function summary
Hyaluronan and proteoglycan link protein 3 integrates into the extracellular matrix by forming part of a complex network essential for tissue structure and integrity. HAPLN3 contributes to the stabilization of matrix macromolecules directly influencing cell adhesion migration and proliferation. It ensures the structural rigidity necessary for normal tissue functions and provides the necessary dynamic balance for tissue repair and maintenance.
- Pathways
Hyaluronan and proteoglycan link protein 3 participates in the formation and remodeling of the extracellular matrix pathway important for processes like embryogenesis and wound healing. It interacts with proteins such as aggrecan and versican which are also key components of the matrix regulatory network. Additionally HAPLN3 is involved with the hyaluronan metabolism pathway assisting in maintaining homeostasis of tissue hydration and elasticity.
- Associated diseases and disorders
Hyaluronan and proteoglycan link protein 3 has associations with osteoarthritis where its expression affects cartilage degradation and regeneration. It is also connected to neurological disorders due to its expression in the brain where it may interact with neurocan. Aberrant regulation or mutation of HAPLN3 can lead to disrupted extracellular matrix integrity contributing to the pathophysiology of these conditions.
Product promise
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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
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Terms & Conditions.
2 product images
Sanger Sequencing - Human HAPLN3 knockout A549 cell line (ab267058)
Allele-1: 4 bp deletion in exon3
Sanger Sequencing - Human HAPLN3 knockout A549 cell line (ab267058)
Allele-2: 1 bp insertion in exon 3.
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