Anti-FOXP1 antibody [EPR4113]
- 20ul selling size
- RabMAb
- Recombinant
- Advanced Validation
- 각 태그의 뜻
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(12 제품이 사용된 논문 )
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-FOXP1 antibody [EPR4113] (AB134055)
Immunocytochemistry/ Immunofluorescence analysis of MCF7 (Human breast adenocarcinoma epithelial cell) cells labeling FOXP1 with purified ab134055 at 1/500 dilution (0.4 μg/ml). Cells were fixed in 4% Paraformaldehyde and permeabilized with 0.1% tritonX-100. Cells were counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) at 1 : 200 (2.5 μg/ml). Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) was used as the secondary antibody at 1/1000 (2 μg/ml) dilution. DAPI (blue) was used as nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-FOXP1 antibody [EPR4113] (AB134055)
Intracellular Flow Cytometry analysis of Daudi (human Burkitt's lymphoma) cells labeling FOXP1 with purified ab134055 at 1/200 dilution (1ug/ml) (red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. A Goat anti rabbit IgG (Alexa Fluor® 488) (1/2000 dilution) was used as the secondary antibody. Rabbit monoclonal IgG (Black) was used as the isotype control, cells without incubation with primary antibody and secondary antibody (Blue) were used as the unlabeled control.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FOXP1 antibody [EPR4113] (AB134055)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Human diffuse large B-cell lymphoma tissue sections labeling FOXP1 with purified ab134055 at 1/1000 dilution (0.21 μg/ml). Heat mediated antigen retrieval was performed using ab93684 (Tris/EDTA buffer, pH 9.0). ImmunoHistoProbe one step HRP Polymer (ready to use) was used as the secondary antibody. Negative control : PBS instead of the primary antibody. Hematoxylin was used as a counterstain.
- ChIP-seq
Lab
ChIP-sequencing - Anti-FOXP1 antibody [EPR4113] (AB134055)
Chromatin was prepared from K-562 cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 107 cells and 8 µg of ab134055 [EPR4113]. 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-FOXP1 antibody [EPR4113] (AB134055)
Chromatin was prepared from K-562 cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 107 cells and 8 µg of ab134055 [EPR4113]. 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-FOXP1 antibody [EPR4113] (AB134055)
Chromatin was prepared from K-562 cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 107 cells and 8 µg of ab134055 [EPR4113]. 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-FOXP1 antibody [EPR4113] (AB134055)
Chromatin was prepared from MEF cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 5 x 10^6 cells and 4 µg of ab134055 [EPR4113]. 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-FOXP1 antibody [EPR4113] (AB134055)
Chromatin was prepared from MEF cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 5 x 10^6 cells and 4 µg of ab134055 [EPR4113]. 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-FOXP1 antibody [EPR4113] (AB134055)
Chromatin was prepared from MEF cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 5 x 10^6 cells and 4 µg of ab134055 [EPR4113]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The Input control is also shown.
- WB
Lab
Western blot - Anti-FOXP1 antibody [EPR4113] (AB134055)
The multiple bands are consistent with what have been described in the literature PMID : 12692134.
All lanes:
Western blot - Anti-FOXP1 antibody [EPR4113] (ab134055) at 1/1000 dilution
Lane 1:
Daudi (Human Burkitt's lymphoma lymphoblast) whole cell lysates at 20 µg
Lane 2:
RAW264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysates at 20 µg
Lane 3:
Mouse lung cell lysates at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/ko/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 75 kDa
Observed band size: 50 kDa,70 kDa,95 kDa
false
- WB
Lab
Western blot - Anti-FOXP1 antibody [EPR4113] (AB134055)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/1000,000 dilution.
Lysate was freshly made and used for Western blotting immediately to minimize protein degradation.
All lanes:
Western blot - Anti-FOXP1 antibody [EPR4113] (ab134055) at 1/1000 dilution
Lane 1:
HEK 293 (human embryonic kidney epithelial cell) whole cell lysate (Frozen) at 20 µg
Lane 2:
HEK 293 (human embryonic kidney epithelial cell) whole cell lysate (Fresh) at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/20000 dilution
Observed band size: 90 kDa,70 kDa,36 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-FOXP1 antibody [EPR4113] (AB134055)
The multiple bands are consistent with what have been described in the literature PMID : 12692134.
All lanes:
Western blot - Anti-FOXP1 antibody [EPR4113] (ab134055) at 1/5000 dilution
All lanes:
2.4G2 (Rat B cell lymphoma B lymphocyte) whole cell lysates at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/ko/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 75 kDa
Observed band size: 50 kDa,70 kDa,95 kDa
false
관련 conjugated 항체와 다양한 조성의 항체 (8)
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Anti-FOXP1 antibody [EPR4113] - BSA and Azide free
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660 APC
APC Anti-FOXP1 antibody [EPR4113]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-FOXP1 antibody [EPR4113]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-FOXP1 antibody [EPR4113]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-FOXP1 antibody [EPR4113]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-FOXP1 antibody [EPR4113]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-FOXP1 antibody [EPR4113]
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578 PE
PE Anti-FOXP1 antibody [EPR4113]
Reactivity 정보
제품 세부 정보
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.
특성 및 보관 정보
제형
Purification 테크닉
보관 버퍼
배송 시 보관 조건
적절한 단기 보관 기간
적절한 단기 보관 조건
적절한 장기 보관 조건
분주 정보
보관 정보
추가 정보
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
This transcription factor functions in the regulation of gene expression associated with neurodevelopment cardiac growth and immune responses. FOXP1 often forms a complex with other transcription factors such as FOXP2 and FOXP4 which enhances its regulatory roles. These interactions allow it to control various genetic programs that are important in the maturation and specification of different cell types. Moreover FOXP1 contributes to the modulation of B-cell development and function highlighting its importance in immune system regulation.
Pathways
FOXP1 takes part in several key signaling pathways including the Wnt signaling pathway and the TGF-beta pathway. The Wnt signaling pathway relates FOXP1 to β-catenin influencing the expression of genes involved in cell proliferation and differentiation. In the TGF-beta pathway its interactions with SMAD proteins underline its function in cellular processes such as apoptosis and epithelial–mesenchymal transition. These pathways emphasize FOXP1's contribution to controlling cell growth and development across different biological contexts.
제품 프로토콜
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타겟 정보
대체 명칭 보기
제품이 사용된 논문 (12)
Recent publications for all applications. Explore the 전체 목록and refine your search
Communications biology 8:431 PubMed40082538
2025
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Genomics, proteomics & bioinformatics 22: PubMed38902848
2024
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MedComm 4:e411 PubMed38020715
2023
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Phytotherapy research : PTR 38:1745-1760 PubMed37740455
2023
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Experimental and therapeutic medicine 26:450 PubMed37614418
2023
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Journal of gynecologic oncology 33:e81 PubMed36335987
2022
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Annals of translational medicine 10:583 PubMed35722379
2022
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American journal of translational research 13:4360-4375 PubMed34150019
2021
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Journal of cellular and molecular medicine 24:12513-12524 PubMed32996692
2020
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The Journal of comparative neurology 526:1235-1266 PubMed29297931
2018
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IHC-P
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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