Anti-SARS-CoV-2 nsp15 antibody [EPR24840-74] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal R1AB antibody. Carrier free. Suitable for ICC/IF, Flow Cyt, IHC-P, WB, I-ELISA and reacts with Recombinant full length protein - SARS-CoV-2, SARS-CoV-2 samples.
View Alternative Names
1a-1b, rep, Replicase polyprotein 1ab, pp1ab, ORF1ab polyprotein, 1a-1b, rep, Replicase polyprotein 1ab, pp1ab, ORF1ab polyprotein
- Flow Cyt
Lab
Flow Cytometry - Anti-SARS-CoV-2 nsp15 antibody [EPR24840-74] - BSA and Azide free (AB284630)
This data was developed using ab284629, the same antibody clone in a different buffer formulation.
Flow Cytometry analysis of HEK-293T (Human embryonic kidney epithelial cell) cells transfected with a SARS-CoV-2 nsp9 (Left) or SARS-CoV2 nsp15 (Right) expression vector containing a myc tag labeling SARS-CoV2 nsp15 with ab284629 at 1/500 dilution (left and right). Cells were fixed with 4% Paraformaldehyde and permeabilised with 90% Methanol. A Goat anti-rabbit IgG (Alexa Fluor® 488, ab150081) secondary antibody was used at 1/5000 dilution. Alexa Fluor® 647 Anti-Myc tag antibody [9E10] (ab223895) was used to label transfected cells.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SARS-CoV-2 nsp15 antibody [EPR24840-74] - BSA and Azide free (AB284630)
This data was developed using ab284629, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of Paraffin-embedded sections of human tonsil tissue labelling SARS-CoV-2 NSP15 with ab284629 at 1/100 dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Counter stained with Haematoxylin. Secondary antibody only control : Used PBS instead of primary antibody
Negative control : no staining on human tonsil.
The section was incubated with ab284629 for 30 mins at room temperature. Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 1 (pH 6.0) for 20 minutes.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SARS-CoV-2 nsp15 antibody [EPR24840-74] - BSA and Azide free (AB284630)
This data was developed using ab284629, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of Paraffin-embedded sections A) HEK-293T transfected with SARS-CoV2 NSP15 expression vector containing a his tag (B) HEK-293T transfected with SARS-CoV-2 NSP9 expression vector containing a his tag labelling SARS-CoV-2 NSP15 with ab284629 at 1/100 dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Counter stained with Haematoxylin. Secondary antibody only control : Used PBS instead of primary antibody
Positive staining on HEK-293T transfected with SARS-CoV2 NSP15 expression vector containing a his tag (Image A); No staining on HEK-293T SARS-CoV-2 NSP9 expression vector containing a his tag. (Image B).
The section was incubated with ab284629 for 30 mins at room temperature. Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 1 (pH 6.0) for 20 minutes.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-SARS-CoV-2 nsp15 antibody [EPR24840-74] - BSA and Azide free (AB284630)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) cells labelling SARS-CoV2 nsp15 with primary antibody anti-SARS-CoV-2 nsp15 antibody (ab284629) at 1/500 dilution, followed by AlexaFluor®488 Goat anti-Rabbit secondary antibody (green) (ab150081) at 1/1000 dilution. Myc-Tag Mouse mab (Alexa Fluor® 647) (red) was used to counterstain at 1/100 dilution. The nuclear counter stain is DAPI (blue).
Confocal image showing positive staining in HEK-293T cells transfected with a SARS-CoV2 nsp15 expression vector containing a myc tag, and no staining in HEK-293T cells transfected with a SARS-CoV2 nsp9 expression vector containing a myc tag. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
This data was developed using ab284629, the same antibody clone in a different buffer formulation.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SARS-CoV-2 nsp15 antibody [EPR24840-74] - BSA and Azide free (AB284630)
This data was developed using ab284629, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of Paraffin-embedded sections of rat spleen tissue labelling SARS-CoV-2 NSP15 with ab284629 at 1/100 dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Counter stained with Haematoxylin. Secondary antibody only control : Used PBS instead of primary antibody
Negative control : no staining on rat spleen.
The section was incubated with ab284629 for 30 mins at room temperature. Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 1 (pH 6.0) for 20 minutes.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SARS-CoV-2 nsp15 antibody [EPR24840-74] - BSA and Azide free (AB284630)
This data was developed using ab284629, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of Paraffin-embedded sections of mouse spleen tissue labelling SARS-CoV-2 NSP15 with ab284629 at 1/100 dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Counter stained with Haematoxylin. Secondary antibody only control : Used PBS instead of primary antibody
Negative control : no staining on mouse spleen.
The section was incubated with ab284629 for 30 mins at room temperature. Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 1 (pH 6.0) for 20 minutes.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
- I-ELISA
Lab
Indirect ELISA - Anti-SARS-CoV-2 nsp15 antibody [EPR24840-74] - BSA and Azide free (AB284630)
This data was developed using ab284629, the same antibody clone in a different buffer formulation.
Indirect ELISA showing primary antibody ab284629 binding to recombinant SARS-COV-2 NSP15 His-tag protein. Plates were coated with recombinant SARS-COV-2 NSP15 His-tag protein and recombinant SARS-COV-2 NSP9 His-tag protein at 1000 ng/ml. Binding of ab284629 was assessed in a serial dilution range 0.016- 1000 ng/ml (a 3-fold serial dilution).
Binding was detected using pre-adsorbed secondary antibody, goat anti-rabbit IgG H&L (HRP, ab97080) at 1/2000 dilution.
- WB
Lab
Western blot - Anti-SARS-CoV-2 nsp15 antibody [EPR24840-74] - BSA and Azide free (AB284630)
This data was developed using ab284629, the same antibody clone in a different buffer formulation.
ab284630 was shown to bind specifically to SARS-CoV-2 NSP15 protein in Western blot.
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.
Blocking buffer : 3% milk in TBS-0.1% Tween® 20 (TBS-T)
Lanes 1 - 2:
Western blot - Anti-SARS-CoV-2 nsp15 antibody [EPR24840-74] (<a href='/en-us/products/primary-antibodies/sars-cov-2-nsp15-antibody-epr24840-74-ab284629'>ab284629</a>)
Lanes 3 - 4:
Western blot - Anti-SARS-CoV-2 nsp15 antibody [EPR24840-74] (<a href='/en-us/products/primary-antibodies/sars-cov-2-nsp15-antibody-epr24840-74-ab284629'>ab284629</a>) at 1/1000 dilution
Lanes 1 and 3:
Recombinant SARS-CoV2 NSP15 protein (His tagged) at 0.1 µg
Lanes 2 and 4:
Recombinant SARS-CoV2 NSP15 protein (His tagged) at 0.05 µg
Secondary
Lanes 1 - 2:
Western blot - Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-mouse-igg-h-l-irdye-680rd-preadsorbed-ab216776'>ab216776</a>) at 1/20000 dilution
Lanes 3 - 4:
Western blot - Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>) at 1/20000 dilution
Predicted band size: 40 kDa
Observed band size: 40 kDa
false
Reactivity data
Product details
ab284630 is a carrier free version of ab284629.
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
Nsp15 is an important participant in the viral replication machinery of SARS-CoV-2. Nsp15 as part of the replication and transcription complex processes viral RNA to promote efficient replication. This protein may interact indirectly with other non-structural proteins such as nsp8 and nsp12 which form part of the RNA-dependent RNA polymerase complex. By maintaining the integrity of viral RNA nsp15 ensures successful virus propagation.
Pathways
Nsp15 plays a significant role in the viral life cycle particularly in the genome replication and transcription pathways. This protein is connected to nsp10 and nsp14 which are involved in RNA proofreading and capping. These interactions support the virus in overcoming innate immune responses by ensuring proper RNA processing and replication. Through these pathways nsp15 contributes significantly to the viral survival and proliferation within the host.
Product protocols
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Target data
Additional targets
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