重组Anti-FOXK1/MNF抗体[EPR27320-65] - BSA and Azide free
Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- Advanced Validation
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Rabbit Recombinant Monoclonal FOXK1/MNF antibody. Carrier free. Suitable for ChIP-seq, WB, IHC-P, ICC/IF, Flow Cyt (Intra), IP and reacts with Human, Mouse, Rat samples.
查看别名
MNF, FOXK1, Forkhead box protein K1, Myocyte nuclear factor
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. Flow cytometric analysis of K-562 (human chronic myelogenous leukemia lymphoblast) cells labelling FOXK1/MNF with ab309510 at 1/500 dilution (0.1 ug)/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 1/5000 dilution was used as the secondary antibody.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized K-562 (human chronic myelogenous leukemia lymphoblast) cells labelling FOXK1/MNF with ab309510 at 1/50 (10.34 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/mL dilution (Green). Confocal image showing nuclear staining in K-562 cell line.Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8). 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 2 ug/mL dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human colon carcinom tissue labeling FOXK1/MNF with ab309510 at 1/2000 (0.259 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on human colon carcinoma (PMID : 27223064, PMID : 28623323). The section was incubated with ab309510 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 was performed 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-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling FOXK1/MNF with ab309510 at 1/2000 (0.259 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on human colon. The section was incubated with ab309510 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- ChIP-seq
Lab
ChIP-sequencing - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using the same antibody clone in a different buffer formulation (ab309510).
Chromatin was prepared from HeLa cells. Cells were fixed with 1.5 mM EGS for 30 min, combined with 1% formaldehyde for 10 min. ChIP was performed with 107 cells and 8 µg of ab309510 [EPR27320-65]. 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-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using the same antibody clone in a different buffer formulation (ab309510).
Chromatin was prepared from HeLa cells. Cells were fixed with 1.5 mM EGS for 30 min, combined with 1% formaldehyde for 10 min. ChIP was performed with 107 cells and 8 µg of ab309510 [EPR27320-65]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The input control is also shown.
- IP
Supplier Data
Immunoprecipitation - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. FOXK1/MNF was immunoprecipitated from 0.35 mg HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate with ab309510 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab309510 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate Lane 2 : ab309510 IP in HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab309510 in HeLa whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 84 seconds Lysate was freshly made and used for Immunoprecipitation immediately to minimize protein degradation.
All lanes:
Immunoprecipitation - Anti-FOXK1/MNF antibody [EPR27320-65] (<a href='/products/primary-antibodies/foxk1-mnf-antibody-epr27320-65-ab309510'>ab309510</a>) at 1/30 dilution
All lanes:
HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 84s
- ChIP-seq
Lab
ChIP-sequencing - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using the same antibody clone in a different buffer formulation (ab309510).
Chromatin was prepared from HeLa cells. Cells were fixed with 1.5 mM EGS for 30 min, combined with 1% formaldehyde for 10 min. ChIP was performed with 107 cells and 8 µg of ab309510 [EPR27320-65]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The input control is also shown.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse colon tissue labeling FOXK1/MNF with ab309510 at 1/2000 (0.259 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on mouse colon. The section was incubated with ab309510 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 was performed 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-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labeling FOXK1/MNF with ab309510 at 1/2000 (0.259 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on rat cerebrum.The section was incubated with ab309510 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 was performed 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-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling FOXK1/MNF with ab309510 at 1/2000 (0.259 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on mouse cerebrum.The section was incubated with ab309510 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized NIH/3T3 (mouse embryonic fibroblast) cells labelling FOXK1/MNF with ab309510 at 1/50 (10.34 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/mL dilution (Green). Confocal image showing nuclear staining in NIH/3T3 cell line.Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8). 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 2 ug/mL dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. Flow cytometric analysis of NIH/3T3 (mouse embryonic fibroblast) cells labelling FOXK1/MNF with ab309510 at 1/500 dilution (0.1 ug)/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 1/5000 dilution was used as the secondary antibody.
- IP
Supplier Data
Immunoprecipitation - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. FOXK1/MNF was immunoprecipitated from 0.35 mg NIH/3T3 (mouse embryonic fibroblast) whole cell lysate with ab309510 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab309510 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : NIH/3T3 (mouse embryonic fibroblast) whole cell lysate Lane 2 : ab309510 IP in NIH/3T3 (mouse embryonic fibroblast) whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab309510 in NIH/3T3 whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 3 minutes Lysate was freshly made and used for Immunoprecipitation immediately to minimize protein degradation.
All lanes:
Immunoprecipitation - Anti-FOXK1/MNF antibody [EPR27320-65] (<a href='/products/primary-antibodies/foxk1-mnf-antibody-epr27320-65-ab309510'>ab309510</a>) at 1/30 dilution
All lanes:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 81 seconds
All lanes:
Western blot - Anti-FOXK1/MNF antibody [EPR27320-65] (<a href='/products/primary-antibodies/foxk1-mnf-antibody-epr27320-65-ab309510'>ab309510</a>) at 1/1000 dilution
Lane 1:
K-562 (human chronic myelogenous leukemia lymphoblast) transfected with scrambled siRNA control whole cell lysate at 20 µg
Lane 2:
K-562 transfected with siRNA specifically targeti FOXK1/MNF whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 95 kDa
false
Exposure time: 81s
- WB
Supplier Data
Western blot - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Lysates were freshly made and used for Western blotting immediately to minimize protein degradation. Exposure time : 147 seconds
All lanes:
Western blot - Anti-FOXK1/MNF antibody [EPR27320-65] (<a href='/products/primary-antibodies/foxk1-mnf-antibody-epr27320-65-ab309510'>ab309510</a>) at 1/1000 dilution
Lane 1:
HepG2 (human hepatocellar carcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg
Lane 4:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 5:
PC-12 (rat adrenal gland pheochromocytoma cell) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 95 kDa
false
Exposure time: 147s
- WB
Supplier Data
Western blot - Anti-FOXK1/MNF antibody [EPR27320-65] - BSA and Azide free (AB309511)
This data was developed using ab309510, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Lysates were freshly made and used for Western blotting immediately to minimize protein degradation. Exposure time : 3 minutes
All lanes:
Western blot - Anti-FOXK1/MNF antibody [EPR27320-65] (<a href='/products/primary-antibodies/foxk1-mnf-antibody-epr27320-65-ab309510'>ab309510</a>) at 1/1000 dilution
Lane 1:
Rat brain tissue lysate at 20 µg
Lane 2:
Rat liver tissue lysate at 20 µg
Lane 3:
Mouse brain tissue lysate at 20 µg
Lane 4:
Mouse liver tissue lysate at 20 µg
Lane 5:
Mouse testis tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 95 kDa
false
Exposure time: 3min
不同偶联物与剂型 (2)
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Anti-FOXK1/MNF antibody [EPR27320-65]
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-FOXK1/MNF antibody [EPR27320-65]
反应性数据
产品详情
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.
性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存条件
推荐的长期储存条件
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
FOXK1/MNF is involved in the regulation of cell cycle progression and muscle regeneration. It forms part of a transcriptional complex that modulates gene expression to control these processes. In muscle tissue FOXK1/MNF influences the activation of satellite cells which are necessary for muscle repair and growth. This protein’s function in regulating cellular proliferation highlights its significance in tissue development and regeneration.
Pathways
The FOXK1/MNF protein is instrumental in the Wnt signaling and PI3K/AKT pathways. These pathways are significant for controlling cell proliferation differentiation and survival. Within these pathways FOXK1/MNF interacts with proteins such as beta-catenin in the Wnt signaling pathway. Through these interactions it modulates the transcription of genes responsible for various cellular functions further underlining its role in tissue regeneration and cancer development.
产品实验方案
- Visit the General protocols
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靶点信息
Abcam 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