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AB324222

Human VIL1 Knockout A549 cell line

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VIL1 KO cell line available to order. KO validated by Western blot. Free of charge wild type control available. Deletion. To order both knockout and wild-type control cells: select '2 x 1000000 Cells/vial'. To order only knockout cells: select '1000000 Cells/vial'.
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Sanger Sequencing - Human VIL1 Knockout A549 cell line (AB324222)
  • Sanger seq

Lab

Sanger Sequencing - Human VIL1 Knockout A549 cell line (AB324222)

256 bp deletion after Val148 (edit 1); 190 bp deletion and 1 bp deletion after Val148 (edit 2)

Western blot - Human VIL1 Knockout A549 cell line (AB324222)
  • WB

Lab

Western blot - Human VIL1 Knockout A549 cell line (AB324222)

Western blot : Anti-VIL1 antibody [EPR3491(3)] (ab133510) staining at 1/5000 dilution, shown in green; Mouse anti-Alpha Tubulin [DM1A] (ab7291) loading control staining at 1/20000 dilution, shown in magenta. In Western blot, ab133510 was shown to bind specifically to VIL1. A band was observed at 93 kDa in wild-type A549 cell lysates with no signal observed at this size in VIL1 knockout cell line. To generate this image, wild-type and VIL1 knockout A549 cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3 % milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution.

All lanes:

Western blot - Anti-Villin antibody [EPR3491(3)] (<a href='/ko/products/primary-antibodies/villin-antibody-epr34913-ab133510'>ab133510</a>) at 1/5000 dilution

Lane 1:

Wild-type A549 cell lysate at 20 µg

Lanes 2 and 4:

Empty cell lysate at 20 µg

Lane 3:

Western blot - Human VIL1 Knockout A549 cell line (ab324222) at 20 µg

Lane 5:

HepG2 cell lysate at 20 µg

Lane 6:

Jurkat Nuclear 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: 93 kDa

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주요 정보

세포 유형

A549

Species or organism

Human

조직

Lung

제형

Liquid

form

Knockout 검증

Western blot

Mutation 정보

Deletion

질병

Carcinoma

Reactivity 정보

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "WB": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "Sanger seq": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" } } }

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

{ "values": { "2x1000000Cellsvial": { "sellingSize": "2 x 1000000 Cells/vial", "publicAssetCode":"ab324222-2x1000000Cells_vial", "assetComponentDetails": [ { "size":"1 x 1000000 Cells/vial", "name":"Human wild type A549 cell line component", "number":"AB324222-CMP02" }, { "size":"1 x 1000000 Cells/vial", "name":"Human VIL1 Knockout A549 cell line component", "number":"AB324222-CMP01" } ] }, "1000000Cellsvial": { "sellingSize": "1000000 Cells/vial", "publicAssetCode":"ab324222-1000000Cells_vial", "assetComponentDetails": [ { "size":"1 x 1000000 Cells/vial", "name":"Human VIL1 Knockout A549 cell line component", "number":"AB324222-CMP01", "productcode":"" } ] } } }

특성 및 보관 정보

유전자명
VIL1
유전자 편집 종류
Knockout
유전자 편집 방식
CRISPR technology
Knockout 검증
Western blot
배송 시 보관 조건
Dry Ice
적절한 단기 보관 기간
A few days
적절한 단기 보관 조건
-196°C
적절한 장기 보관 조건
-196°C

Cell culture

Biosafety level

EU: 1 US: 1

Adherent/suspension

Adherent

Gender

Male

Viability

>= 60%

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.
  • Do not allow the cell density to exceed 7x104 cells/cm2.
배양 배지

F-12K + 10% FBS

동결보존 배지

Cell Freezing Medium-DMSO Serum free media, contains 8.7% DMSO in MEM supplemented with methyl cellulose.

제품 프로토콜

Product promise

저희는 고품질 시약으로 고객님의 연구를 서포트하고자 최선을 다하고 있으며, 모든 단계에서 함께 하겠습니다. 만약 제품이 기대한 성능을 보이지 않을 경우에도 Product Promise로 보호받으실 수 있습니다.
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