Anti-Daxx antibody [E94] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
- What is this?
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(4 Publications)
Knockout Tested Rabbit Recombinant Monoclonal DAXX antibody. Carrier free. Suitable for IHC-P, WB and reacts with Human, Mouse, Rat samples. Cited in 4 publications.
View Alternative Names
BING2, DAP6, DAXX, Death domain-associated protein 6, Daxx, ETS1-associated protein 1, Fas death domain-associated protein, hDaxx, EAP1
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Daxx antibody [E94] - BSA and Azide free (AB239806)
ab32140, at a dilution of 1/50, staining Daxx in paraffin embedded human stomach adenocarcinoma tissue by Immunohistochemistry.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab32140).
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- WB
Lab
Western blot - Anti-Daxx antibody [E94] - BSA and Azide free (AB239806)
All lanes:
Western blot - Anti-Daxx antibody [E94] - BSA and Azide free (ab239806)
Lane 1:
Wild-type HAP1 whole cell lysate at 20 µg
Lane 2:
DAXX knockout HAP1 whole cell lysate at 20 µg
Predicted band size: 81 kDa
false
- WB
Lab
Western blot - Anti-Daxx antibody [E94] - BSA and Azide free (AB239806)
This data was developed using the same antibody clone in a different buffer formulation (ab32140).
Lanes 1- 2 : Merged signal (red and green). Green - ab32140 observed at 100 kDa. Red - Anti-GAPDH antibody [6C5] - Loading Control (ab8245) observed at 37 kDa.
ab32140 was shown to react with Daxx in wild-type HeLa cells in western blot. Loss of signal was observed when knockout cell line ab265233 (knockout cell lysate ab257408) was used. Wild-type HeLa and DAXX knockout HeLa cell lysates were subjected to SDS-PAGE. Membrane was blocked for 1 hour at room temperature in 0.1% TBST with 3% non-fat dried milk. ab32140 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) overnight at 4°C at a 1 in 5000 dilution and a 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye®800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye®680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-Daxx antibody [E94] (<a href='/en-us/products/primary-antibodies/daxx-antibody-e94-ab32140'>ab32140</a>) at 1/5000 dilution
Lane 1:
Wild-type HeLa cell lysate at 20 µg
Lane 2:
DAXX knockout HeLa cell lysate at 20 µg
Lane 2:
Western blot - Human DAXX knockout HeLa cell line (<a href='/en-us/products/cell-lines/human-daxx-knockout-hela-cell-line-ab265233'>ab265233</a>)
Predicted band size: 81 kDa
Observed band size: 100 kDa
false
- WB
Lab
Western blot - Anti-Daxx antibody [E94] - BSA and Azide free (AB239806)
This data was developed using the same antibody clone in a different buffer formulation (ab32140). False colour image of Western blot : Anti-Daxx antibody [E94] staining at 1/5000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab32140 was shown to bind specifically to Daxx. A band was observed at 105 kDa in wild-type A549 cell lysates with no signal observed at this size in DAXX knockout cell line. To generate this image, wild-type and DAXX 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.
Lanes 1 - 3:
Western blot - Anti-Daxx antibody [E94] (<a href='/en-us/products/primary-antibodies/daxx-antibody-e94-ab32140'>ab32140</a>) at 1/5000 dilution
Lanes 1 - 3:
Western blot - Anti-Daxx antibody [E94] - BSA and Azide free (ab239806) at 1/5000 dilution
Lane 1:
Wild-type A549 cell lysate at 20 µg
Lane 2:
Western blot - Human DAXX knockout A549 cell line (<a href='/en-us/products/cell-lines/human-daxx-knockout-a549-cell-line-ab287356'>ab287356</a>)
Lane 2:
DAXX knockout A549 cell lysate at 20 µg
Lane 3:
THP-1 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
false
- WB
Lab
Western blot - Anti-Daxx antibody [E94] - BSA and Azide free (AB239806)
This data was developed using the same antibody clone in a different buffer formulation (ab32140). False colour image of Western blot : Anti-Daxx antibody [E94] staining at 1/5000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab32140 was shown to bind specifically to Daxx. A band was observed at 100 kDa in wild-type HCT 116 cell lysates with no signal observed at this size in DAXX knockout cell line. To generate this image, wild-type and DAXX knockout HCT 116 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-Daxx antibody [E94] (<a href='/en-us/products/primary-antibodies/daxx-antibody-e94-ab32140'>ab32140</a>) at 1/5000 dilution
Lane 1:
Wild-type HCT 116 cell lysate at 20 µg
Lane 2:
Western blot - Human DAXX knockout HCT116 cell line (<a href='/en-us/products/cell-lines/human-daxx-knockout-hct116-cell-line-ab287355'>ab287355</a>)
Lane 2:
DAXX knockout HCT 116 cell lysate at 20 µg
Lane 3:
THP-1 cell lysate at 20 µg
Lane 4:
K562 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: 81 kDa
Observed band size: 100 kDa
false
- WB
Supplier Data
Western blot - Anti-Daxx antibody [E94] - BSA and Azide free (AB239806)
False colour image of Western blot : Anti-Daxx antibody [E94] staining at 1/5000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab32140 was shown to bind specifically to Daxx. A band was observed at 105 kDa in wild-type MCF7 cell lysates with no signal observed at this size in DAXX knockout cell line. To generate this image, wild-type and DAXX knockout MCF7 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-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution. This data was developed using the same antibody clone in a different buffer formulation (ab32140).
All lanes:
Western blot - Anti-Daxx antibody [E94] (<a href='/en-us/products/primary-antibodies/daxx-antibody-e94-ab32140'>ab32140</a>) at 1/5000 dilution
Lane 1:
Wild-type MCF7 cell lysate at 20 µg
Lane 2:
DAXX knockout MCF7 cell lysate at 20 µg
Lane 3:
THP-1 cell lysate at 20 µg
Lane 4:
K562 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: 81 kDa
Observed band size: 105 kDa
false
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Reactivity data
Product details
ab239806 is the carrier-free version of ab32140.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Product protocols
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Target data
Publications (4)
Recent publications for all applications. Explore the full list and refine your search
Nature communications 16:6009 PubMed40593805
2025
Applications
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Species
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Biomedicines 12: PubMed39200236
2024
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Species
Unspecified reactive species
International journal of molecular sciences 23: PubMed35955489
2022
Applications
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Species
Unspecified reactive species
PeerJ 8:e9203 PubMed32596036
2020
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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