Anti-DDX17 antibody [EPR13807(B)] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
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Rabbit Recombinant Monoclonal DDX17 antibody. Carrier free. Suitable for IHC-P, ICC/IF, WB, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples.
View Alternative Names
Probable ATP-dependent RNA helicase DDX17, DEAD box protein 17, DEAD box protein p72, DEAD box protein p82, RNA-dependent helicase p72, DDX17
- WB
Lab
Western blot - Anti-DDX17 antibody [EPR13807(B)] - BSA and Azide free (AB250190)
This data was developed using ab180190, the same antibody clone in a different buffer formulation.
Lanes 1 - 4 : Merged signal (red and green). Green - ab180190 observed at 72 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab180190 was shown to recognize DDX17 in wild-type HEK 293 cells as signal was lost at the expected MW in DDX17 knockout cells. Additional cross-reactive bands were observed in the wild-type and knockout cells. Wild-type and DDX17 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% Milk. ab180190 and ab8245 (Mouse anti-GAPDH loading control) were incubated overnight at 4°C at 1/5000 dilution and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-DDX17 antibody [EPR13807(B)] (<a href='/en-us/products/primary-antibodies/ddx17-antibody-epr13807b-ab180190'>ab180190</a>) at 1/5000 dilution
Lane 1:
Wild-type HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 20 µg
Lane 2:
DDX17 knockout HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 20 µg
Lane 2:
Western blot - Human DDX17 knockout HEK-293 cell line (<a href='/en-us/products/cell-lines/human-ddx17-knockout-hek-293-cell-line-ab261721'>ab261721</a>)
Lane 3:
HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Predicted band size: 72 kDa
false
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-DDX17 antibody [EPR13807(B)] - BSA and Azide free (AB250190)
This data was developed using ab250190, the same antibody clone in a different buffer formulation.
Flow Cytometry analysis of J774A.1 (Mouse reticulum cell sarcoma monocyte macrophage, Left) / NIH/3T3 (Mouse embryonic fibroblast, Right) cells labelling DDX17 with Purified ab250190 at 1 : 20 dilution (10μg/ml) (Red). Cells were fixed with 4% Paraformaldehyde and permeabilised with 90% Methanol. A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) secondary antibody was used at 1 : 2000. Isotype control - Rabbit monoclonal IgG (Black). Unlabelled control - Cell without incubation with primary antibody and secondary antibody (Blue).
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-DDX17 antibody [EPR13807(B)] - BSA and Azide free (AB250190)
This data was developed using ab250190, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of MCF7 (Human breast adenocarcinoma epithelial cell) cells labeling DDX17 with Purified ab250190 at 1 : 50 dilution (2 μg/ml). Cells were fixed in 100% Methanol and permeabilized with 0.1% tritonX-100. Cells were counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) 1 : 200 (2.5 μg/ml). Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) was used as the secondary antibody at 1 : 1000 (2 μg/ml) dilution. DAPI (blue) was used as nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-DDX17 antibody [EPR13807(B)] - BSA and Azide free (AB250190)
This data was developed using ab180190, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of rat testis tissue sections labeling DDX17 with Purified ab180190 at 1 : 5000 dilution (0.02 μg/ml). Heat mediated antigen retrieval was performed using . Tissue was counterstained with Hematoxylin. Perform heat mediated antigen retrieval using ab93684 (Tris/EDTA buffer, pH 9.0) secondary antibody was used at 1 : 0 dilution. PBS instead of the primary antibody was used as the negative control.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-DDX17 antibody [EPR13807(B)] - BSA and Azide free (AB250190)
This data was developed using ab180190, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human breast carcinoma tissue sections labeling DDX17 with Purified ab180190 at 1 : 5000 dilution (0.02 μg/ml). Heat mediated antigen retrieval was performed using . Tissue was counterstained with Hematoxylin. Perform heat mediated antigen retrieval using ab93684 (Tris/EDTA buffer, pH 9.0) secondary antibody was used at 1 : 0 dilution. PBS instead of the primary antibody was used as the negative control.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-DDX17 antibody [EPR13807(B)] - BSA and Azide free (AB250190)
This data was developed using ab180190, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of mouse testis tissue sections labeling DDX17 with Purified ab180190 at 1 : 5000 dilution (0.02 μg/ml). Heat mediated antigen retrieval was performed using . Tissue was counterstained with Hematoxylin. Perform heat mediated antigen retrieval using ab93684 (Tris/EDTA buffer, pH 9.0) secondary antibody was used at 1 : 0 dilution. PBS instead of the primary antibody was used as the negative control.
- WB
Unknown
Western blot - Anti-DDX17 antibody [EPR13807(B)] - BSA and Azide free (AB250190)
All lanes:
Western blot - Anti-DDX17 antibody [EPR13807(B)] (<a href='/en-us/products/primary-antibodies/ddx17-antibody-epr13807b-ab180190'>ab180190</a>) at 1/1000 dilution
Lane 1:
HEK-293 (Human embryonic kidney epithelial cell) whole cell lysate at 20 µg
Lane 2:
MCF7 (Human breast adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
Rat brain lysate at 20 µg
Lane 4:
Rat testis lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 72 kDa
false
- WB
Lab
Western blot - Anti-DDX17 antibody [EPR13807(B)] - BSA and Azide free (AB250190)
This data was developed using ab180190, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure time : 6 seconds.
All lanes:
Western blot - Anti-DDX17 antibody [EPR13807(B)] (<a href='/en-us/products/primary-antibodies/ddx17-antibody-epr13807b-ab180190'>ab180190</a>) at 1/1000 dilution
Lane 1:
HeLa (Human colorectal adenocarcinoma epithelial cell) cell lysate at 10 µg
Lane 2:
Mouse embryo lysate at 10 µg
Lane 3:
NIH/3T3 (Mouse embryonic fibroblast) cell lysate at 10 µg
Lane 4:
J774A.1 (Mouse reticulum cell sarcoma monocyte macrophage) cell lysate at 10 µg
Lane 5:
RAW264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) cell lysate at 10 µg
Lane 6:
C2C12 (Mouse myoblasts myoblast) cell lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 72 kDa
Observed band size: 72 kDa
false
Related conjugates and formulations (1)
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Anti-DDX17 antibody [EPR13807(B)]
Reactivity data
Product details
ab250190 is the carrier-free version of ab180190.
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
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
This enzyme plays a significant role in RNA metabolism. DDX17 is part of the spliceosome complex which is essential for splicing pre-mRNA into mature mRNA. Through its helicase activity DDX17 ensures the proper remodeling of RNA structures which is necessary for accurate splicing. The protein also contributes to the regulation of gene expression and has been observed to influence transcription factors.
Pathways
RNA processing and maturation are key biological functions of DDX17. The protein integrates into the mRNA splicing pathway where it orchestrates proper RNA folding and splice site selection. Furthermore DDX17 interacts with other DEAD-box proteins such as DDX5 to assist in chromatin remodeling and transcription regulation facilitating efficient gene expression.
Product protocols
- Visit the General protocols
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Target data
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