Creative Biolabs

Human ADAM17 Knockout HeLa Cell Line

[CAT#: NCL2008ZP577]

Human ADAM17 knockout cell line

Cell Assay
Cell Types:

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This is a human ADAM17 gene knockout HeLa cell line which achieved by using CRISPR/Cas9 gene editing technology.
Recommended control cell line: human wild-type HeLa cell line (ab255928)

Cryopreservation cell culture medium: Cell Freezing Medium-DMSO serum-free medium supplemented with 10% (v/v) DMSO
Cell Types
Cell Location
Cell Assay
Application Notes
To use as WB control, resuspend the lyophilizate in 50 µL of LDS* Sample Buffer to have a final concentration of 2 mg/ml. For reducing conditions, we recommend a final concentration of 0.1 M DTT.

*Usage of SDS sample buffer is not recommended with these lyophilized lysates.
Mutation Description
Knockout achieved by using CRISPR/Cas9, 11 bp deletion in exon 5 and 2 bp deletion in exon 5
Passage Number
Knockout Validation
Sanger Sequencing
Relevant Diseases
Neurological Disorders
Research Areas
Alzheimer's Disease Signaling
Tangles & Tau
1 x 10e6 cells/vial, 1 mL
Constituents: 8.7% DMSO, 2% Cellulose, methyl ether
Cell State
Live cells are in mid log-phase growth.
Growth Pattern
STR Analysis
Amelogenin X D5S818: 11, 12 D13S317: 12, 13.3 D7S820: 8, 12 D16S539: 9, 10 vWA: 16, 18 TH01: 7 TPOX: 8, 12 CSF1PO: 9, 10
Biosafety Level
Tissue Source
Cell Purity
Cell Viability
Antibiotic Resistance
Puromycin 1.00µg/ml
Mycoplasma Testing
Sterility Testing
Sterility testing was performed in accordance with USP and EP regulations. All of our sterility testing is performed in an isolator or clean room environments. The cell line has been screened using the membrane filtration testing methods to confirm the absence of aerobic, anaerobic and fungi microorganisms.
Genetic Stability Testing
Cell genetic stability study was perfomed under ICH guidelines. We provide guidance on the appropriate testing program upon your requirements.
Dry ice
Shipped on Dry Ice. Store in liquid nitrogen.
Handling Advice
Upon arrival, the sample vial should be stored in liquid nitrogen vapor phase instead of -80°C. Storage at -80°C will cause loss of vitality.

1. Thaw the vial in a 37°C water bath for about 1-2 minutes.
2. Transfer the cell suspension to a 15 mL conical tube containing pre-warmed 5 mL complete medium DMEM + 10% FBS, and rotate 125 x g for about 5 minutes at room temperature.
3. Resuspend the cell pellet with 1 mL of pre-warmed complete medium DMEM + 10% FBS, and distribute it into a 25 cm2 culture flask, which contains 10 mL of pre-warmed complete medium DMEM + 10% FBS.
4. Incubate the culture with 5% CO2 in a 37°C incubator.
5. The recommended subculture ratio is 1:4-1:6. When cells grow at 80-90% confluence and divide, the cells should be passaged.
Research Use Only
For research use only, not for diagnostic or therapeutic use.
Store in gas phase of liquid nitrogen immediately upon receipt. This product is stable for 6 months when stored as directed.
Quality Control
Mycoplasma was tested for sterility, post-freezing viability, and short-term repeat (STR) analysis for cell line identification. Cytochrome oxidase I (COI) was analyzed for cell line species identification.
Official Name
Full Name
ADAM Metallopeptidase Domain 17
Alternative Names
ADAM Metallopeptidase Domain 17; Tumor Necrosis Factor; Alpha; Converting Enzyme; Snake Venom-Like Protease; TNF-Alpha Convertase; EC; TACE; CSVP; Disintegrin And Metalloproteinase Domain-Containing Protein 17; ADAM Metallopeptidase Domain 18;
Gene ID
6868 (Human); 11491 (Mouse)
Uniprot ID
P78536 (Human); Q9Z0F8 (Mouse)
For Research Use Only. Not For Clinical Use.
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