Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free)
- BOND RX™ Validated
- RabMAb
- Recombinant
- Advanced Validation
- What is this?
Be the first to review this product! Submit a review
|
(0 Publication)
Rabbit Recombinant Monoclonal Ikaros antibody. Carrier free. Suitable for WB, IHC-P, IHC-Fr, Flow Cyt (Intra), IP, ChIP-seq and reacts with Human, Mouse, Rat samples.
View Alternative Names
IK1, IKAROS, LYF1, ZNFN1A1, IKZF1, DNA-binding protein Ikaros, Ikaros family zinc finger protein 1, Lymphoid transcription factor LyF-1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded Human thymus tissue labeling Ikaros with ab300405 at 1/2000 (0.27 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on human thymus (PMID : 8964602).The section was incubated with ab300405 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) was used.Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation.Flow cytometric analysis of HeLa (human cervix adenocarcinoma epithelial cell, Left) / Jurkat (human T cell leukemia T lymphocyte, Right) cells labelling Ikaros with ab300405 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody. Negative control : HeLa(HPA data)
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded Human spleen tissue labeling Ikaros with ab300405 at 1/2000 (0.27 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on human spleen (PMID : 8964602).The section was incubated with ab300405 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) was used.Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IP
Supplier Data
Immunoprecipitation - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation.
Ikaros was immunoprecipitated from 0.35 mg Raji (human burkitt's lymphoma b lymphocyte) whole cell lysate 10 ug with ab300405 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab300405 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : Raji (human burkitt's lymphoma b lymphocyte) whole cell lysate 10 ug
Lane 2 : ab300405 IP in Raji whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab300405 in Raji whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 8 seconds.
Lanes 1 - 3:
Immunoprecipitation - Anti-Ikaros antibody [EPR25259-176] (<a href='/en-us/products/primary-antibodies/ikaros-antibody-epr25259-176-ab300405'>ab300405</a>) at 1/1000 dilution
Lanes 1 - 3:
Immunoprecipitation - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (ab300417)
All lanes:
Raji whole cell lysate at 10 µg
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 8s
- ChIP-seq
Lab
ChIP-sequencing - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using the same antibody clone in a different buffer formulation (ab300405).
Chromatin was prepared from Raji cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 107 cells and 8 µg of ab300405 [EPR25259-176]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The input control is also shown.
- ChIP-seq
Lab
ChIP-sequencing - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using the same antibody clone in a different buffer formulation (ab300405).
Chromatin was prepared from Raji cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 107 cells and 8 µg of ab300405 [EPR25259-176]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The input control is also shown.
- ChIP-seq
Lab
ChIP-sequencing - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using the same antibody clone in a different buffer formulation (ab300405).
Chromatin was prepared from Raji cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 107 cells and 8 µg of ab300405 [EPR25259-176]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The input control is also shown.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse thymus (fresh) tissue labeling Ikaros with ab300405 at 1/100 (5.39 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Positive staining on mouse thymus is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labeling Ikaros with ab300405 at 1/2000 (0.27 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on mouse spleen.The section was incubated with ab300405 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) was used.Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded Rat spleen tissue labeling Ikaros with ab300405 at 1/2000 (0.27 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on rat spleen.The section was incubated with ab300405 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) was used.Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse kidney (fresh) tissue labeling Ikaros with ab300405 at 1/100 (5.39 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Negative control (PMID : 1439790)No staining on mouse kidney is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat kidney (fresh) tissue labeling Ikaros with ab300405 at 1/100 (5.39 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Negative control (PMID : 1439790)No staining on rat kidney is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat thymus (fresh) tissue labeling Ikaros with ab300405 at 1/100 (5.39 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Positive staining on rat thymus is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation.Flow cytometric analysis of EL4 (mouse lymphoma T lymphocyte) cells labelling Ikaros with ab300405 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
- IP
Supplier Data
Immunoprecipitation - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation.
Ikaros was immunoprecipitated from 0.35 mg EL4 (mouse lymphoma t lymphocyte) whole cell lysate 10 ug with ab300405 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab300405 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : EL4 (mouse lymphoma t lymphocyte) whole cell lysate 10 ug
Lane 2 : ab300405 IP in EL4 whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab300405 in EL4 whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 8 seconds.
Lanes 1 - 3:
Immunoprecipitation - Anti-Ikaros antibody [EPR25259-176] (<a href='/en-us/products/primary-antibodies/ikaros-antibody-epr25259-176-ab300405'>ab300405</a>) at 1/1000 dilution
Lanes 1 - 3:
Immunoprecipitation - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (ab300417)
All lanes:
EL4 whole cell lysate at 10 µg
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 8s
- WB
Supplier Data
Western blot - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation. Blocking Buffer and concentration : 5% NFDM/TBST
All lanes:
Western blot - Anti-Ikaros antibody [EPR25259-176] (<a href='/en-us/products/primary-antibodies/ikaros-antibody-epr25259-176-ab300405'>ab300405</a>) at 1/1000 dilution
Lane 1:
Jurkat (human T cell leukemia cell line from peripheral blood) whole cell lysate
Lane 2:
Raji (human burkitts lymphoma b lymphocyte) whole cell lysate
Lane 3:
Daudi (human burkitts lymphoma lymphoblast) whole cell lysate
Lane 4:
HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate
Lane 5:
EL4 (mouse lymphoma t lymphocyte) whole cell lysate
Lane 6:
Mouse spleen tissue lysate
Lane 7:
Mouse thymus tissue lysate
Lane 8:
Mouse kidney tissue lysate
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 1/100000 dilution
Observed band size: 30 kDa,70 kDa
false
- WB
Supplier Data
Western blot - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation. Blocking Buffer and concentration : 5% NFDM/TBST
All lanes:
Western blot - Anti-Ikaros antibody [EPR25259-176] (<a href='/en-us/products/primary-antibodies/ikaros-antibody-epr25259-176-ab300405'>ab300405</a>) at 1/1000 dilution
Lane 1:
His-tagged human Ikaros/IKZF1 recombinant protein
Lane 2:
GST-tagged human Helios/IKZF2 recombinant protein
Lane 3:
GST-tagged human Aiolos/IKZF3 recombinant protein
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 1/100000 dilution
Observed band size: 16 kDa
false
Exposure time: 3s
- WB
Supplier Data
Western blot - Anti-Ikaros antibody [EPR25259-176] (BSA and Azide free) (AB300417)
This data was developed using ab300405, the same antibody clone in a different buffer formulation. Blocking Buffer and concentration : 5% NFDM/TBST
All lanes:
Western blot - Anti-Ikaros antibody [EPR25259-176] (<a href='/en-us/products/primary-antibodies/ikaros-antibody-epr25259-176-ab300405'>ab300405</a>) at 1/1000 dilution
Lane 1:
Rat thymus tissue lysate
Lane 2:
Rat spleen tissue lysate
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 1/100000 dilution
Observed band size: 30 kDa,70 kDa
false
Exposure time: 70s
Reactivity data
Product details
ab300417 is a carrier free version of ab300405.
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.
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.
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.
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
Ikaros protein functions in the regulation of lymphoid cell development. It is a part of a chromatin-remodeling complex influencing chromatin accessibility. Through its zinc finger domains it binds to specific DNA sequences controlling genes necessary for lymphocyte differentiation and proliferation. Ikaros influences various cell types within the immune system especially affecting T and B cell development and also regulates cytokine receptor genes necessary for proper immune function.
Pathways
The Ikaros protein is critical to lymphocyte signaling pathways particularly the JAK/STAT and NF-κB pathways. In these pathways Ikaros interacts with other transcription factors like GATA3 and STAT5 integrating signals that are important for immune cell function and development. This integration allows a coordinated response to extracellular signals ensuring effective immune responses or tolerance.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
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