Human CDH1 (E Cadherin) knockout A-431 cell line
Human CDH1 (E Cadherin) knockout A-431 cell line
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CDH1 KO cell line available to order. KO validated by Next Generation Sequencing, Western blot. Free of charge wild type control available. Knockout achieved by CRISPR/Cas9; X = 1 bp insertion after Phe38 (allele 1), 4 bp deletion after Thr37 (allele 2), and 1 bp deletion after Thr37 (allele 3) of the WT protein Frameshift = 95%. To order both knockout and wild-type control cells: select '2 x 1000000 Cells/vial'. To order only knockout cells: select '1000000 Cells/vial'.
別名を表示する
Arc 1, CADH1_HUMAN, CAM 120/80, CD 324, CD324 antigen, CDH1, CDHE, Cadherin-1, E-Cad/CTF3, E-cadherin, ECAD, Epithelial cadherin, LCAM, Liver cell adhesion molecule, UVO, Uvomorulin, cadherin 1 type 1 E-cadherin, epithelial calcium dependant adhesion protein
- WB
Lab
Western blot - Human CDH1 (E Cadherin) knockout A-431 cell line (AB273747)
Lanes 1 - 4:
Western blot - Anti-E Cadherin antibody [SP64] (<a href='/products/primary-antibodies/e-cadherin-antibody-sp64-ab227639'>ab227639</a>) at 1/100 dilution
Lanes 1 - 4:
Western blot - Anti-E Cadherin antibody [SP64] - BSA and Azide free (<a href='/products/primary-antibodies/e-cadherin-antibody-sp64-bsa-and-azide-free-ab240984'>ab240984</a>) at 1/100 dilution
Lane 1:
Wild-type A431 cell lysate at 20 µg
Lane 2:
Western blot - Human CDH1 (E Cadherin) knockout A-431 cell line (ab273747)
Lane 2:
Western blot - Human CDH1 (E Cadherin) knockout A-431 cell lysate (ab273781)
Lane 2:
CDH1 knockout A431 cell lysate at 20 µg
Lane 3:
MCF7 cell lysate at 20 µg
Lane 4:
MDA-MB-231 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: 105 kDa,130 kDa
false
- WB
Lab
Western blot - Human CDH1 (E Cadherin) knockout A-431 cell line (AB273747)
Lanes 1 - 4:
Western blot - Anti-E Cadherin antibody [EP700Y] - Intercellular Junction Marker (<a href='/products/primary-antibodies/e-cadherin-antibody-ep700y-intercellular-junction-marker-ab40772'>ab40772</a>) at 1/10000 dilution
Lanes 1 - 4:
Western blot - Anti-E Cadherin antibody [EP700Y] - Low endotoxin, Azide free (<a href='/products/primary-antibodies/e-cadherin-antibody-ep700y-low-endotoxin-azide-free-ab201499'>ab201499</a>) at 1/10000 dilution
Lanes 1 - 4:
Western blot - Anti-E Cadherin antibody [EP700Y] - BSA and Azide free (<a href='/products/primary-antibodies/e-cadherin-antibody-ep700y-bsa-and-azide-free-ab256580'>ab256580</a>) at 1/10000 dilution
Lane 1:
Wild-type Raji cell lysate at 20 µg
Lane 2:
Western blot - Human CDH1 (E Cadherin) knockout A-431 cell line (ab273747)
Lane 2:
Western blot - Human CDH1 (E Cadherin) knockout A-431 cell lysate (ab273781)
Lane 2:
CDH1 knockout Raji cell lysate at 20 µg
Lane 3:
MCF7 cell lysate at 20 µg
Lane 4:
MDA-MB-231 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: 105 kDa,130 kDa
false
- WB
Lab
Western blot - Human CDH1 (E Cadherin) knockout A-431 cell line (AB273747)
Western blot : Anti-CDH1 antibody [4A2] (ab231303) staining at 1 ug/ml, shown in green; Rabbit Anti-GAPDH antibody [EPR16891] (ab181602) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab231303 was shown to bind specifically to CDH1. A band was observed at 130, 110, 55 kDa in wild-type A431 cell lysates with no signal observed at this size in CDH1 knockout cell line ab273747 (knockout cell lysate ab273781). To generate this image, wild-type and CDH1 knockout A431 cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 5 % 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-Mouse IgG H&L 800CW and Goat anti-Rabbit IgG H&L 680RD at 1/20000 dilution.
All lanes:
Western blot - Anti-E Cadherin antibody [4A2] (<a href='/products/primary-antibodies/e-cadherin-antibody-4a2-ab231303'>ab231303</a>) at 1 µg/mL
Lane 1:
Wild-type A431 cell lysate at 20 µg
Lane 2:
Western blot - Human CDH1 (E Cadherin) knockout A-431 cell lysate (ab273781)
Lane 2:
Western blot - Human CDH1 (E Cadherin) knockout A-431 cell line (ab273747)
Lane 2:
CDH1 knockout A431 cell lysate at 20 µg
Lane 3:
Caco-2 cell lysate at 20 µg
Secondary
All lanes:
Goat anti-Mouse IgG H&L 800CW and Goat anti-Rabbit IgG H&L 680RD at 1/20000 dilution
Predicted band size: 97 kDa
false
- WB
Lab
Western blot - Human CDH1 (E Cadherin) knockout A-431 cell line (AB273747)
Western blot : Anti-CDH1 antibody [EP700Y] (ab40772) staining at 1/1000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab40772 was shown to bind specifically to CDH1. A band was observed at 130, 110, 80, 55, 40 kDa in wild-type A431 cell lysates with no signal observed at this size in CDH1 knockout cell line ab273747 (knockout cell lysate ab273781). To generate this image, wild-type and CDH1 knockout A431 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-E Cadherin antibody [EP700Y] - Intercellular Junction Marker (<a href='/products/primary-antibodies/e-cadherin-antibody-ep700y-intercellular-junction-marker-ab40772'>ab40772</a>) at 1/1000 dilution
Lane 1:
Wild-type A431 cell lysate at 20 µg
Lane 2:
Western blot - Human CDH1 (E Cadherin) knockout A-431 cell lysate (ab273781)
Lane 2:
Western blot - Human CDH1 (E Cadherin) knockout A-431 cell line (ab273747)
Lane 2:
CDH1 knockout A431 cell lysate at 20 µg
Lane 3:
Caco-2 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
Predicted band size: 97 kDa
false
- NGS
Lab
Next Generation Sequencing - Human CDH1 (E Cadherin) knockout A-431 cell line (AB273747)
1 bp insertion after Phe38 (allele 1), 4 bp deletion after Thr37 (allele 2), and 1 bp deletion after Thr37 (allele 3) of the WT protein
Reactivity data
製品の詳細
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.
製品内容
出荷温度及び保存条件
遺伝子名
遺伝子編集のタイプ
遺伝子編集の方法
ノックアウト検証方法
出荷温度
短期保存期間
短期保存温度
長期保存温度
取り扱い方法
初回取り扱いガイドライン
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.
継代培養ガイドライン
- 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.
培養培地
DMEM (High Glucose) + 10% FBS
凍結保存培地
Cell Freezing Medium-DMSO Serum free media, contains 8.7% DMSO in MEM supplemented with methyl cellulose.
補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
E-Cadherin participates in establishing and maintaining adherens junctions which are vital for tissue structure. E-Cadherin operates as a core component of the cadherin-catenin complex which links the protein to the actin cytoskeleton. Through this linkage E-Cadherin plays an important role in signaling pathways that influence cellular growth and differentiation. The protein's ability to mediate intercellular connections also regulates cellular motility and supports basic aspects of cell behavior in epithelial tissues.
Pathways
E-Cadherin influences both the Wnt signaling pathway and the epithelial-to-mesenchymal transition (EMT). Within the Wnt signaling pathway E-Cadherin partners with β-catenin a significant player in transcription regulation and cell signaling. Disruption in E-Cadherin's adhesive functionality can lead to increased β-catenin availability affecting downstream transcriptional control. In the EMT process E-Cadherin loss characterizes an important step in which cells gain migratory and invasive properties typically seen during metastasis in cancer progression.
Quality control
STR analysis
CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX
Cell culture
Biosafety level
EU: 1 US: 1
Adherent/suspension
Adherent
Gender
Female
ターゲットの情報
Abcam 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