Anti-DDX17 antibody [EPR13807(B)] - C-terminal (ab180190)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR13807(B)] to DDX17 - C-terminal
- Suitable for: ICC/IF, Flow Cyt, IHC-P, WB
- Knockout validated
- Reacts with: Mouse, Human
Overview
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Product name
Anti-DDX17 antibody [EPR13807(B)] - C-terminal
See all DDX17 primary antibodies -
Description
Rabbit monoclonal [EPR13807(B)] to DDX17 - C-terminal -
Host species
Rabbit -
Tested Applications & Species
See all applications and species dataApplication Species Flow Cyt HumanICC/IF HumanIHC-P HumanWB MouseHuman -
Immunogen
Synthetic peptide within Human DDX17 aa 100-200 (Cysteine residue). The exact sequence is proprietary.
Database link: Q92841 -
Positive control
- WB: HeLa, NIH/3T3, J774A.1, RAW264.7, C2C12, 293T, HeLa and MCF7 cell lysates; Mouse embryo lysate. IHC-P: Human breast tissue. ICC/IF: 293T and MCF7 cells. Flow Cyt: MCF7 cells.
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General notes
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species. Please contact us for more information.
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 production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
We are constantly working hard to ensure we provide our customers with best in class antibodies. As a result of this work we are pleased to now offer this antibody in purified format. We are in the process of updating our datasheets. The purified format is designated 'PUR' on our product labels. If you have any questions regarding this update, please contact our Scientific Support team.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle. -
Storage buffer
pH: 7.20
Preservative: 0.01% Sodium azide
Constituents: 9% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA, 50% Tissue culture supernatant -
Concentration information loading...
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Purity
Tissue culture supernatant -
Clonality
Monoclonal -
Clone number
EPR13807(B) -
Isotype
IgG -
Research areas
Images
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All lanes : Anti-DDX17 antibody [EPR13807(B)] - C-terminal (ab180190) at 1/5000 dilution
Lane 1 : Wild-type HEK 293 whole cell lysate
Lane 2 : DDX17 knockout HEK 293 whole cell lysate
Lane 3 : Hela whole cell lysate
Lysates/proteins at 20 µg per lane.
Predicted band size: 72 kDaLanes 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.
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ab180190 staining DDX17 antibody in MCF-7 (human breast carcinoma) cells by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with 4% PFA and permeabilised with 0.1% triton X-100. Samples were incubated with primary antibody at a dilution of 1/500. A goat anti rabbit IgG (Alexa Fluor® 488) (ab150077) was used as the secondary antibody at a dilution of 1/1000. DAPI was used as a nuclear counterstain.
Negative control 1:PBS only.
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Immunohistochemical analysis of paraffin embedded Human breast tissue labeling DDX17 with ab180190 at 1/100.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
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Flow Cytometrical analysis of permeabilized MCF7 cells labeling DDX17 with ab180190 at 1/10 (red) or a rabbit IgG negative (green).
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All lanes : Anti-DDX17 antibody [EPR13807(B)] - C-terminal (ab180190) at 1/1000 dilution
Lane 1 : HeLa (Human colorectal adenocarcinoma epithelial cell) cell lysate
Lane 2 : Mouse embryo lysate
Lane 3 : NIH/3T3 (Mouse embryonic fibroblast) cell lysate
Lane 4 : J774A.1 (Mouse reticulum cell sarcoma monocyte macrophage) cell lysate
Lane 5 : RAW264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) cell lysate
Lane 6 : C2C12 (Mouse myoblasts myoblast) cell lysate
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution
Predicted band size: 72 kDa
Observed band size: 72 kDaBlocking and diluting buffer and concentration: 5% NFDM/TBST
Exposure time: 6 s
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All lanes : Anti-DDX17 antibody [EPR13807(B)] - C-terminal (ab180190) at 1/1000 dilution
Lane 1 : 293T cell lysate
Lane 2 : HeLa cell lysate
Lane 3 : MCF7 cell lysate
Secondary
All lanes : HRP labelled goat anti-rabbit at 1/2000 dilution
Predicted band size: 72 kDa
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Immunofluorescent analysis of 293T cells labeling DDX17 with ab180190 at 1/100.
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