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AB258402

Human DYRK1A knockout HEK-293T cell lysate

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DYRK1A KO cell lysate available now. KO validated by. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon12.

View Alternative Names

DYR1A_HUMAN, DYRK, DYRK 1, DYRKA, Dual specificity YAK 1 related kinase, Dual specificity YAK1-related kinase, Dual specificity tyrosine (Y) phosphorylation regulated kinase 1A, Dual specificity tyrosine phosphorylation regulated kinase, Dual specificity tyrosine phosphorylation regulated kinase 1, Dual specificity tyrosine-phosphorylation-regulated kinase 1A, HP 86, MNB, MNB protein kinase, MNB protein kinase, Serine/threonine-specific, MNB/DYRK protein kinase, MNBH, MRD7, Minibrain (Drosophila) homolog, Minibrain homolog, Minibrain, Drosophila, homolog of, Mnb protein kinase homolog hp86, OTTHUMP00000109090, OTTHUMP00000109091, OTTHUMP00000109094, OTTHUMP00000174799, Protein kinase minibrain homolog, Serine/threonine kinase MNB, hMNB

3 Images
Western blot - Human DYRK1A knockout HEK-293T cell lysate (AB258402)
  • WB

Lab

Western blot - Human DYRK1A knockout HEK-293T cell lysate (AB258402)

Lane 1 : Wild-type HEK-293T cell lysate 20 μg
Lane 2 : HEK-293T cell lysate 20 μg
Lane 3 : HT1080 cell lysate 20 μg
False colour image of Western blot : Anti-DYRK1A antibody staining at 1/500 dilution, shown in green; Rabbit Anti-GAPDH antibody [EPR16891] (ab181602) loading control staining at 1/20000 dilution, shown in red. In Western blot, the antibody was shown to bind specifically to DYRK1A. A band was observed at 80/95/90 kDa in wild-type HEK-293T cell lysates with no signal observed at this size in DYRK1A knockout cell line ab267336 (knockout cell lysate ab258402). To generate this image, wild-type and DYRK1A knockout HEK-293T 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-Mouse IgG H&L (IRDye® 800CW) preabsorbed (ab216772) and Goat anti-Rabbit IgG H&L (IRDye® 680RD) preabsorbed (ab216777) at 1/20000 dilution.

All lanes:

Anti-DYRK1A antibody at 1/500 dilution

Lane 1:

Wild-type HEK-293T cell lysate at 20 µg

Lane 2:

HEK-293T cell lysate at 20 µg

Lane 2:

Western blot - Human DYRK1A knockout HEK-293T cell line (<a href='/en-us/products/cell-lines/human-dyrk1a-knockout-hek-293t-cell-line-ab267336'>ab267336</a>)

Lane 3:

HT1080 cell lysate at 20 µg

false

Western blot - Human DYRK1A knockout HEK-293T cell lysate (AB258402)
  • WB

Lab

Western blot - Human DYRK1A knockout HEK-293T cell lysate (AB258402)

Lane 1 : Wild-type HEK-293T cell lysate 20 μg
Lane 2 : DYRK1A CRISPR-Cas9 edited HEK-293T cell lysate 20 μg
Lane 3 : HT1080 cell lysate 20 μg
Lane 4 : U-251 MG cell lysate 20 μg
False colour image of Western blot : Anti-DYRK1A antibody [EPR24132-61] staining at 1/2000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab259869 was shown to bind specifically to DYRK1A. A band was observed at 80/85/90 kDa in wild-type HEK-293T cell lysates with no signal observed at this size in DYRK1A CRISPR-Cas9 edited cell line ab267336 (CRISPR-Cas9 edited cell lysate ab258402). The band observed in the CRISPR-Cas9 edited lysate lane below 80/85/90 kDa is likely to represent a truncated form of DYRK1A. This has not been investigated further and the functional properties of the gene product have not been determined. To generate this image, wild-type and DYRK1A CRISPR-Cas9 edited HEK-293T 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 (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) at 1/20000 dilution.

All lanes:

Western blot - Anti-DYRK1A antibody [EPR24132-61] (<a href='/en-us/products/primary-antibodies/dyrk1a-antibody-epr24132-61-ab259869'>ab259869</a>) at 1/2000 dilution

Lane 1:

Wild-type HEK-293T cell lysate at 20 µg

Lane 2:

DYRK1A CRISPR-Cas9 edited HEK-293T cell lysate at 20 µg

Lane 2:

Western blot - Human DYRK1A knockout HEK-293T cell line (<a href='/en-us/products/cell-lines/human-dyrk1a-knockout-hek-293t-cell-line-ab267336'>ab267336</a>)

Lane 3:

HT1080 cell lysate at 20 µg

Lane 4:

U-251 MG cell lysate at 20 µg

Secondary

All lanes:

Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (<a href='/en-us/products/secondary-antibodies/goat-mouse-igg-h-l-irdye-680rd-preadsorbed-ab216776'>ab216776</a>) at 1/20000 dilution

Predicted band size: 86 kDa

Observed band size: 80 kDa,85 kDa,90 kDa

false

Sanger Sequencing - Human DYRK1A knockout HEK-293T cell lysate (AB258402)
  • Sanger seq

Unknown

Sanger Sequencing - Human DYRK1A knockout HEK-293T cell lysate (AB258402)

Homozygous : 1 bp insertion in exon12

Key facts

Cell type

HEK-293T

Species or organism

Human

Tissue

Kidney

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon12.

Reactivity data

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Product details

Knockout cell lysate achieved by CRISPR/Cas9.

REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

Lysate preparation: Our lysates are made using RIPA buffer to which we add a protease inhibitor cocktail and phosphatase inhibitor cocktail (ratio: 300:100:10). This means that the protein of interest is denatured. If you require a native form of the protein please use the live cell version. Please refer to our lysis protocol for further details on how our lysates are prepared.

User storage instructions: Lyophilizate may be stored at 4°C. After reconstitution, store at -20°C for short-term storage or -80°C for long-term storage.

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.

What's included?

{ "values": { "1Kit": { "sellingSize": "1 Kit", "publicAssetCode":"ab258402-1Kit", "assetComponentDetails": [ { "size":"1 x 100 µg", "name":"Human DYRK1A knockout HEK293T cell lysate", "number":"AB258402-CMP01", "productcode":"" }, { "size":"1 x 100 µg", "name":"Human wild-type HEK293T cell lysate", "number":"AB258402-CMP02", "productcode":"" } ] } } }

Properties and storage information

Gene name
DYRK1A
Gene editing type
Knockout
Gene editing method
CRISPR technology
Knockout validation
Sanger Sequencing
Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C

Quality control

STR analysis

CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX

Cell culture

Biosafety level

EU: 2 US: 2

Adherent/suspension

Adherent

Gender

Female

Product protocols

Product promise

We are committed to supporting your work with high-quality reagents, and we're here for you every step of the way. In the unlikely event that one of our products does not perform as expected, you're protected by our Product Promise.
For full details, please see our Terms & Conditions

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

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