Human PTGS1 knockout A-431 cell line
- Advanced Validation
- 각 태그의 뜻
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- WB
Lab
Western blot - Human PTGS1 knockout A-431 cell line (AB270477)
Lanes 1 - 4:
Western blot - Anti-COX1 / Cyclooxygenase 1 antibody [EPR5867] (<a href='/ko/products/primary-antibodies/cox1-cyclooxygenase-1-antibody-epr5867-ab133319'>ab133319</a>) at 1/1000 dilution
Lanes 1 - 4:
Western blot - Anti-COX1 / Cyclooxygenase 1 antibody [EPR5867] - BSA and Azide free (<a href='/ko/products/primary-antibodies/cox1-cyclooxygenase-1-antibody-epr5867-bsa-and-azide-free-ab248471'>ab248471</a>) at 1/1000 dilution
Lane 1:
Wild-type A431 cell lysate at 20 µg
Lane 2:
Western blot - Human PTGS1 knockout A-431 cell line (ab270477) at 20 µg
Lane 2:
Western blot - Human PTGS1 knockout A-431 cell lysate (ab270500) at 20 µg
Lane 2:
PTGS1 knockout A431 cell lysate at 20 µg
Lane 3:
C2C12 cell lysate at 20 µg
Lane 4:
MOLT-4 cell lysate at 20 µg
Secondary
All lanes:
Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution
Observed band size: 70 kDa
false
- WB
Lab
Western blot - Human PTGS1 knockout A-431 cell line (AB270477)
Lanes 1 - 4:
Western blot - Anti-COX1 / Cyclooxygenase 1 antibody [EPR5866] - BSA and Azide free (<a href='/ko/products/primary-antibodies/cox1-cyclooxygenase-1-antibody-epr5866-bsa-and-azide-free-ab219375'>ab219375</a>) at 1/1000 dilution
Lanes 1 - 4:
Western blot - Anti-COX1 / Cyclooxygenase 1 antibody [EPR5866] (<a href='/ko/products/primary-antibodies/cox1-cyclooxygenase-1-antibody-epr5866-ab109025'>ab109025</a>) at 1/1000 dilution
Lane 1:
Wild-type A431 cell lysate at 20 µg
Lane 2:
Western blot - Human PTGS1 knockout A-431 cell lysate (ab270500)
Lane 2:
PTGS1 knockout A431 cell lysate at 20 µg
Lane 2:
Western blot - Human PTGS1 knockout A-431 cell line (ab270477)
Lane 3:
C2C12 cell lysate at 20 µg
Lane 4:
MOLT-4 cell lysate at 20 µg
Secondary
All lanes:
Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution
Observed band size: 70 kDa
false
- NGS
Supplier Data
Next Generation Sequencing - Human PTGS1 knockout A-431 cell line (AB270477)
Knockout achieved by CRISPR/Cas9; X = 28 bp deletion, 2 bp deletion, 1 bp deletion; Frameshift = 99.6%
Reactivity 정보
제품 세부 정보
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.
제품 구성
특성 및 보관 정보
유전자명
유전자 편집 종류
유전자 편집 방식
Knockout 검증
배송 시 보관 조건
적절한 단기 보관 기간
적절한 단기 보관 조건
적절한 장기 보관 조건
추가 정보
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
COX-1 is involved in producing prostaglandins that regulate a variety of normal physiological processes including gastric mucosal protection renal blood flow and platelet aggregation. Unlike COX-2 COX-1 is not induced by inflammatory stimuli and is not part of an inducible complex. It serves to maintain essential physiological functions in various organs and systems making its activity critical for cellular maintenance.
Pathways
COX-1 is primarily involved in the prostaglandin biosynthesis pathway. It converts arachidonic acid into prostaglandin H2 a precursor for other prostaglandins and thromboxanes. Thromboxane A2 produced from this pathway plays an important role in platelet aggregation and vasoconstriction linking COX-1's functions with hemostatic processes. Another protein involved in this pathway is thromboxane synthase which further processes the products of COX-1 activity.
품질 관리
STR analysis
CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX
Cell culture
Biosafety level
EU: 1 US: 1
Adherent/suspension
Adherent
Gender
Female
초기 취급 지침
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. <p>1. Thaw the vial in 37°C water bath for approximately 1-2 minutes.<br>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.<br>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.<br>4. Incubate the culture at 37°C incubator with 5% CO<sub>2</sub>. Check the culture one day after revival and continue to check until 80% confluent. Media change can be given if needed.<br>5. Once confluent passage into an appropriate flask at a density of 2x10<sup>4</sup> cells/cm<sup>2</sup>. Seeding density is given as a guide only and should be scaled to align with individual lab schedules. Cultures should be monitored daily.</p>
Subculture 가이드라인
- 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.
배양 배지
DMEM (High Glucose) + 10% FBS
동결보존 배지
Cell Freezing Medium-DMSO Serum free media, contains 8.7% DMSO in MEM supplemented with methyl cellulose.
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