Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - BSA and Azide free
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal STAT6 phospho Y641 antibody. Carrier free. Suitable for Flow Cyt (Intra), IP, ChIP, Dot, WB and reacts with Human, Mouse, Synthetic peptide, Rat samples. Cited in 1 publication.
View Alternative Names
Signal transducer and transcription activator 6, Stat6
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - BSA and Azide free (AB263949)
Intracellular flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Daudi (Human Burkitt's lymphoma lymphoblast) was serum starved for 24h, then treated with 100ng/ml IL-4 for 15min (Red) / Untreated control (Green) cells labelling STAT6 (phospho Y641) with ab235591 at 1/500 (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). A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab235591).
- IP
Unknown
Immunoprecipitation - Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - BSA and Azide free (AB263949)
STAT6 (phospho Y641) was immunoprecipitated from 0.35 mg Daudi (Human Burkitt's lymphoma lymphoblast) cells serum starved for 24h, then treated with 100ng/ml IL-4 for 15min whole cell lysate, with ab235591 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab235591 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : Daudi cells serum starved for 24h, then treated with 100ng/ml IL-4 for 15min whole cell lysate 10ug
Lane 2 : ab235591 IP in Daudi was serum starved for 24h, then treated with 100ng/ml IL-4 for 15min whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab235591 in Daudi cells serum starved for 24h, then treated with 100ng/ml IL-4 for 15min whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 10 seconds.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab235591).
All lanes:
Immunoprecipitation - Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - ChIP Grade (<a href='/en-us/products/primary-antibodies/stat6-phospho-y641-antibody-epr22599-52-chip-grade-ab235591'>ab235591</a>)
Predicted band size: 94 kDa
false
- ChIP
Unknown
ChIP - Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - BSA and Azide free (AB263949)
Chromatin was prepared from Daudi cells starved for 24h, then treated with hIL-4(100ng/ml, 15min) according to the Abcam Dual-X-ChIP protocol. Cells were fixed with 1.5 mM EGS for 30mins and then formaldehyde for 10min.
The ChIP was performed with 25 μg of chromatin, 5 μg of ab235591 (red), or 5 μg of rabbit normal IgG ab172730 (gray) and 20 μl of Protein A/G sepharose beads. The immunoprecipitated DNA was quantified by real time PCR (Taqman approach for active and inactive loci, Sybr green approach for heterochromatic loci).
Primers and probes are commercial primers from Cell Signaling Technology (Cat. No. : #56554)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab235591).
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - BSA and Azide free (AB263949)
Intracellular flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized RAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) cells was serum starved for 24h, then treated with 100ng/ml IL-4 for 15min (Red) / Untreated control (Green) cells labelling STAT6 (phospho Y641) with ab235591 at 1/500 dilution (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). A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab235591).
- IP
Unknown
Immunoprecipitation - Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - BSA and Azide free (AB263949)
STAT6 (phospho Y641) was immunoprecipitated from 0.35 mg RAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) cells serum starved for 24h, then treated with 100ng/ml IL-4 for 15min whole cell lysate with ab235591 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab235591 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : RAW 264.7 cells serum starved for 24h, then treated with 100ng/ml IL-4 for 15min whole cell lysate 10ug
Lane 2 : ab235591 IP in RAW 264.7 cells serum starved for 24h, then treated with 100ng/ml IL-4 for 15min whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab235591 in RAW 264.7 was serum starved for 24h, then treated with 100ng/ml IL-4 for 15min whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 10 seconds
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab235591).
All lanes:
Immunoprecipitation - Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - ChIP Grade (<a href='/en-us/products/primary-antibodies/stat6-phospho-y641-antibody-epr22599-52-chip-grade-ab235591'>ab235591</a>)
Predicted band size: 94 kDa
false
- Dot
Unknown
Dot Blot - Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - BSA and Azide free (AB263949)
Dot blot analysis using ab235591 at 1/1000 dilution, Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) was used as the secondary antibody at 1/100,000 diluton.
Lane 1 : STAT6 (phospho Y641) peptide (aa636-647).
Lane 2 : STAT6 non-phospho peptide (aa636-647)
Exposure time : 26 seconds.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab235591).
Related conjugates and formulations (7)
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Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - ChIP Grade
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660 APC
APC Anti-STAT6 (phospho Y641) antibody [EPR22599-52] (ChIP Grade)
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - ChIP Grade
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603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - ChIP Grade
-
617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - ChIP Grade
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-STAT6 (phospho Y641) antibody [EPR22599-52] - ChIP Grade
-
578 PE
PE Anti-STAT6 (phospho Y641) antibody [EPR22599-52] (ChIP Grade)
Reactivity data
Product details
ab263949 is the carrier-free version of ab235591.
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
STAT6 plays a central role in the development and function of Th2 cells a subset of T helper cells. The protein controls genes linked to the immune response and inflammation such as IL-4 and IL-13 by binding to specific DNA sequences as part of the transcriptional complex. These processes are critical for antibody class switching in B cells and also for regulating the differentiation of T cells which are processes important in defending against parasitic infections and are linked to allergies.
Pathways
STAT6 functions mainly in the JAK-STAT signaling pathway a pathway important for transmitting information from chemical signals outside cells to the cell nucleus resulting in DNA transcription. Within this pathway STAT6 works closely with JAK1 and JAK3 kinases which phosphorylate STAT6 enabling its activation. The protein also connects with other members of the STAT family like STAT1 and STAT3 during overlapping signaling processes.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Oncology research 30:289-300 PubMed37303493
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'.
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