Anti-IL-33 antibody [EPR17831] - BSA and Azide free
- BOND RX™ Validated
- KO Validated
- RabMAb
- Recombinant
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(2 Publications)
Rabbit Recombinant Monoclonal IL-33 antibody. Carrier free. Suitable for WB, IHC-P, ICC/IF, Flow Cyt (Intra) and reacts with Mouse, Rat samples. Cited in 2 publications.
View Alternative Names
Interleukin-33, IL-33, Il33
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-IL-33 antibody [EPR17831] - BSA and Azide free (AB229698)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized RAW 264.7 (mouse macrophage cell line transformed with Abelson murine leukemia virus) cells labeling IL33 with ab187060 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing increased nuclear staining in RAW 264.7 cells treated with 50 nM Phorbol-12-myristate-13-acetate (PMA) and 5 µg/ml Lipopolysaccharide for 24h.
The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) (ab195889) at 1/200 dilution (red).
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) at 1/1000 dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab187060).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-33 antibody [EPR17831] - BSA and Azide free (AB229698)
Immunohistochemical analysis of paraffin-embedded rat spleen tissue labeling IL33 with ab187060 at 1/2000 dilution, followed by Rabbit specific IHC polymer detection kit HRP/DAB (ab209101), ready to use. Nuclear staining in endothelial cells of rat spleen is observed (PMID : 12819012). Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Rabbit specific IHC polymer detection kit HRP/DAB (ab209101), ready to use.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab187060).
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-IL-33 antibody [EPR17831] - BSA and Azide free (AB229698)
Intracellular Flow Cytometry analysis ofRAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) treated with 50nM PMA and 5�g/ml LPS for 24h (Red) / Untreated control (Green) labeling IL-33 with ab229698 at 1/500 dilution. Goat anti rabbit IgG (Alexa Fluor�488, ab150077) at 1/2000 was used as the secondary antibody. Cells were fixed with4% paraformaldehyde and permeabilised with0.1% Tween-20.Isotype control - Rabbit monoclonal IgG (ab172730) (Black). Unlabelled control - Cell without incubation with primary antibody and secondary antibody (Blue).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-33 antibody [EPR17831] - BSA and Azide free (AB229698)
Immunohistochemical analysis of paraffin-embedded mouse spleen tissue labeling IL33 with ab187060 at 1/2000 dilution, followed by Rabbit specific IHC polymer detection kit HRP/DAB (ab209101), ready to use. Nuclear staining in endothelial cells of mouse spleen is observed (PMID : 12819012). Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Rabbit specific IHC polymer detection kit HRP/DAB (ab209101), ready to use.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab187060).
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-IL-33 antibody [EPR17831] - BSA and Azide free (AB229698)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab187060).
Flow cytometry overlay histogram showing left, Raw264.7 treated with 50nM PMA and 5μg/ml LPS for 24h and right, negative untreated Raw264.7 stained with ab187060 (red line). The cells were fixed with 4% formaldehyde (10 min) and then permeabilised with 0.1% PBS-Triton X-100 for 15 min. The cells were then incubated in 1x PBS containing 10μg/ml anti CD16/CD32 and 10% normal goat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody (ab187060) (1x 106 in 100μl at 1.0μg/ml (1/2090)) for 30min at 22°C.
The secondary antibody Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed was incubated at 1/4000 for 30min at 22°C
Isotype control antibody (black line) was Recombinant Rabbit IgG, monoclonal [EPR25A] - Isotype Control used at the same concentration and conditions as the primary antibody. Unlabelled sample (blue line) was also used as a control.
Acquisition of >5000 events were collected using a 50 mW Blue laser (488nm) and 525/40 bandpass filter.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-33 antibody [EPR17831] - BSA and Azide free (AB229698)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab187060). Immunohistochemical analysis of paraffin-embedded (A) Lymph node tissue from wild-type C57BL/6JGpt mice (B) Lymph node tissue from IL-33 knockout mice labeling IL33 with ab187060 at 1/5000 dilution, followed by LeicaDS9800 (Bond™ Polymer Refine Detection), ready to use. Counter stained with Hematoxylin. Antigen retrieval was heat mediated with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins. Positive staining on (A) Lymph node tissue from wild-type C57BL/6JGpt mice and no staining on (B) Lymph node tissue from IL-33 knockout mice. The section was incubated with ab187060 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and IL33-KO homozygous mice (Strain ID : T052437).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-33 antibody [EPR17831] - BSA and Azide free (AB229698)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab187060). Immunohistochemical analysis of paraffin-embedded (A) Spleen tissue from wild-type C57BL/6JGpt mice (B) Spleen tissue from IL-33 knockout mice labeling IL33 with ab187060 at 1/5000 dilution, followed by LeicaDS9800 (Bond™ Polymer Refine Detection), ready to use. Counter stained with Hematoxylin. Antigen retrieval was heat mediated with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins. Positive staining on (A) Spleen tissue from wild-type C57BL/6JGpt mice and no staining on (B) Spleen tissue from IL-33 knockout mice. The section was incubated with ab187060 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and IL33-KO homozygous mice (Strain ID : T052437).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-33 antibody [EPR17831] - BSA and Azide free (AB229698)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab187060). Immunohistochemical analysis of paraffin-embedded (A) Lung tissue from wild-type C57BL/6JGpt mice (B) Lung tissue from IL-33 knockout mice labeling IL33 with ab187060 at 1/5000 dilution, followed by LeicaDS9800 (Bond™ Polymer Refine Detection), ready to use. Counter stained with Hematoxylin. Antigen retrieval was heat mediated with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins. Positive staining on (A) Lung tissue from wild-type C57BL/6JGpt mice and no staining on (B) Lung tissue from IL-33 knockout mice. The section was incubated with ab187060 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and IL33-KO homozygous mice (Strain ID : T052437).
- WB
Lab
Western blot - Anti-IL-33 antibody [EPR17831] - BSA and Azide free (AB229698)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab187060). Loading control : Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1/200000) (36KDa) Blocking/Diluting buffer and concentration : 5% NFDM/TBST The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and IL33-KO homozygous mice (Strain ID : T052437).
Lanes 1 - 9:
Western blot - Anti-IL-33 antibody [EPR17831] (<a href='/en-us/products/primary-antibodies/il-33-antibody-epr17831-ab187060'>ab187060</a>) at 1/1000 dilution
Lanes 1 - 9:
Western blot - Anti-IL-33 antibody [EPR17831] - BSA and Azide free (ab229698)
Lane 1:
Wild-type mouse spleen tissue lysate (male)
Lanes 2 - 3:
IL-33 knockout spleen tissue lysate (male)
Lane 4:
Wild-type mouse inguinal lymph nodes tissue lysate (male)
Lanes 5 - 6:
IL-33 knockout inguinal lymph nodes tissue lysate (male)
Lane 7:
Wild-type mouse submandibular lymph nodes tissue lysate (male)
Lanes 8 - 9:
IL-33 knockout submandibular lymph nodes tissue lysate (male)
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
Observed band size: 15-30 kDa
false
Exposure time: 38s
- WB
Lab
Western blot - Anti-IL-33 antibody [EPR17831] - BSA and Azide free (AB229698)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab187060). Loading control : Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1/200000) (36KDa) Blocking/Diluting buffer and concentration : 5% NFDM/TBST The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and IL33-KO homozygous mice (Strain ID : T052437).
Lanes 1 - 3:
Western blot - Anti-IL-33 antibody [EPR17831] (<a href='/en-us/products/primary-antibodies/il-33-antibody-epr17831-ab187060'>ab187060</a>)
Lanes 1 - 3:
Western blot - Anti-IL-33 antibody [EPR17831] - BSA and Azide free (ab229698)
Lane 1:
Wild-type mouse lung tissue lysate (male)
Lanes 2 - 3:
IL-33 knockout lung tissue lysate (male)
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
Observed band size: 15-30 kDa
false
Exposure time: 38s
Related conjugates and formulations (4)
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Anti-IL-33 antibody [EPR17831]
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660 APC
APC Anti-IL-33 antibody [EPR17831]
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578 PE
PE Anti-IL-33 antibody [EPR17831]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-IL-33 antibody [EPR17831]
Reactivity data
Product details
ab229698 is the carrier-free version of ab187060.
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 (2)
Recent publications for all applications. Explore the full list and refine your search
Cancer immunology research 8:1381-1392 PubMed32917659
2020
Applications
Unspecified application
Species
Unspecified reactive species
Cell death & disease 9:1173 PubMed30518915
2018
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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