Anti-IL-6 antibody [EPR23819-103] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- What is this?
0
(1 Review)
|
(1 Publication)
Rabbit Recombinant Monoclonal IL-6 antibody. Carrier free. Suitable for IHC-Fr, ICC/IF, WB, IHC-P and reacts with Mouse samples. Cited in 1 publication.
View Alternative Names
Il-6, Il6, Interleukin-6, IL-6, B-cell hybridoma growth factor, Interleukin HP-1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-6 antibody [EPR23819-103] - BSA and Azide free (AB290750)
This data was developed using ab290735, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded (A) HEK-293T cells transfected with mouse IL-6 expression vector containing a his tag, labelling IL-6 with ab290735 at 1/100 (5.75 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on HEK-293T cells transfected with mouse IL-6 expression vector containing a his tag (A). No staining on HEK-293T cells transfected with empty vector containing a his tag (B). The section was incubated with ab290735 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-IL-6 antibody [EPR23819-103] - BSA and Azide free (AB290750)
This data was developed using ab290735, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeilized RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) cells lebelling IL-6 with ab290735 at 1/50 (11.5 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2ug/ml dilution) (Green). Confocal image showing cytoplasmic staining in RAW 264.7 cells treated with LPS (100 ng/ml) for 4h, with addition of BFA (1 ug/ml) for the last 3 hours is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (2.5ug/ml) dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2ug/ml) dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-6 antibody [EPR23819-103] - BSA and Azide free (AB290750)
This data was developed using ab290735, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse lung tissue treated labelling IL-6 with ab290735 at 1/100 (5.75 ug/ml) followed by a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection). Positive staining on Mouse lung treated with lipopolysaccharides (1 ug/ml) for 16 h in vitro (A) and no staining on untreated mouse lung (B) . The section was incubated with ab290735 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-6 antibody [EPR23819-103] - BSA and Azide free (AB290750)
This data was developed using ab290735 the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of formalin fixed paraffin embedded lipopolysaccharide (1 ug/ml) treated mouse lung labelling IL-6 with ab290735 at a concentration of 4µg/ml. The immunostaining was performed on a Ventana DISCOVERY ULTRA (Roche Tissue Diagnostics) instrument with a ChromoMap DAB kit and anti-rabbit HQ and anti-HQ HRP detection. Heat mediated antigen retrieval was performed with DISCOVERY cell conditioning solution (CC1) 100°C, pH8.5 for 32mins. ab290735 Anti-IL-6 antibody [EPR23819-103] was incubated for 16mins at 37°C. Sections were counterstained with Hematoxylin II. Image inset shows absence of staining in untreated tissues. Customers are encouraged to optimise antigen retrieval conditions, antibody concentration, incubation times and temperature for best results in their own IHC assay workflow (automated and manual).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-6 antibody [EPR23819-103] - BSA and Azide free (AB290750)
This data was developed using ab290735, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse spleen treated tissue labelling IL-6 with ab290735 at 1/100 (5.75 ug/ml) followed by a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection)
Positive staining on mouse spleen treated with lipopolysaccharides (1 ug/ml) for 16 h in vitro (A) and no staining on untreated mouse spleen (B). The section was incubated with ab290735 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-IL-6 antibody [EPR23819-103] - BSA and Azide free (AB290750)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized fresh mouse spleen tissue labeling IL-6 with ab290735 at 1/50 dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed secondary at 1/1000. Increased staining on mouse spleen treated with lipopolysaccharide (1 μg/mL) and Brefeldin A (1 μg/mL) for 16 h. The nuclear counterstain was DAPI (Blue). This data was developed using ab290735, the same antibody clone in a different buffer formulation.
- WB
Lab
Western blot - Anti-IL-6 antibody [EPR23819-103] - BSA and Azide free (AB290750)
This data was developed using ab290735, the same antibody clone in a different buffer formulation.
Blocking / Dilution buffer and concentration : 5% NFDM/TBST.
The expression profile/molecular weight observed is consistent with that described in the literature (PMID : 2523818, PMID : 25130514).
IL6 expressed in LPS-induced RAW264.7 cells (PMID : 31718640, PMID : 30823686).
All lanes:
Western blot - Anti-IL-6 antibody [EPR23819-103] (<a href='/en-us/products/primary-antibodies/il-6-antibody-epr23819-103-ab290735'>ab290735</a>) at 1/1000 dilution
Lane 1:
Untreated RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate. at 20 µg
Lane 2:
RAW264.7 treated with 0.1µg/ml lipopolysaccharide (LPS) for 4 hours, then with 1 µg/ml Brefeldin A (BFA) added for 3 hours whole cell 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 1/20 dilution
Predicted band size: 23 kDa
Observed band size: 24 kDa
false
Exposure time: 3min
- WB
Lab
Western blot - Anti-IL-6 antibody [EPR23819-103] - BSA and Azide free (AB290750)
Blocking buffer and concentration : 5% NFDM/TBST
Diluting buffer and concentration : 5% NFDM/TBST
Lanes 1-2 : Anti-IL-6 antibody [EPR23819-103] (ab290735) at 1/1000 dilution
Lanes 3-4 : Anti-IL-6 antibody [EPR21710] (ab229381) at 1/1000 dilution
Lanes 5-6 : Anti-IL-6 antibody [EPR23819-11] (ab259341) at 1/1000 dilution
The expression profile/molecular weight observed is consistent with that described in the literature (PMID : 2523818, PMID : 25130514).
IL-6 expressed in LPS-induced RAW264.7 cells (PMID : 31718640, PMID : 30823686).
Compared with ab290735, ab229381 and ab259341 have higher affinity. We recommend ab229381 or ab259341 as alternatives for western blot.
This data was developed using ab290735, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-IL-6 antibody [EPR23819-103] (<a href='/en-us/products/primary-antibodies/il-6-antibody-epr23819-103-ab290735'>ab290735</a>) at 1/1000 dilution
Lanes 1, 3 and 5:
Untreated RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate at 20 µg
Lanes 2, 4 and 6:
RAW264.7 treated with 0.1µg/ml lipopolysaccharide (LPS) for 4 hours, then with 1 µg/ml Brefeldin A (BFA) added for 3 hours, whole cell 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: 23 kDa
Observed band size: 24 kDa
false
Exposure time: 3min
Reactivity data
Product details
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
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
IL-6 influences immune regulation and acts as part of the acute phase response. It stimulates the production of acute-phase proteins and supports the differentiation of B cells into antibody-producing cells. IL-6 is not known to be part of a larger complex acting primarily as a single entity in signal transduction. Moreover IL-6 impacts the metabolism of iron and bone homeostasis showing its multifunctional nature.
Pathways
IL-6 forms an integral part of several signaling routes particularly the JAK-STAT pathway. In this context IL-6 interacts with signal transducer proteins like STAT3 to transmit signals from the cell surface to the nucleus affecting gene expression. Another important pathway is the MAPK pathway through which IL-6 influences cell proliferation and survival. These interactions reflect IL-6's diverse effects in cellular processes.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Naunyn-Schmiedeberg's archives of pharmacology 396:1461-1470 PubMed36749400
2023
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'.
For licensing inquiries, please contact partnerships@abcam.com