Anti-FUBP1/FBP antibody [EPR12327]
- RabMAb
- Recombinant
- What is this?
5
(2 Reviews)
|
(13 Publications)
Rabbit Recombinant Monoclonal FUBP1/FBP antibody. Suitable for WB, ICC/IF, Flow Cyt (Intra), IHC-P and reacts with Mouse, Rat, Human samples. Cited in 13 publications.
View Alternative Names
Far upstream element-binding protein 1, FBP, FUSE-binding protein 1, DNA helicase V, hDH V, FUBP1
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
Immunocytochemistry/Immunofluorescence analysis of HeLa cells labelling FUBP1/FBP with purified ab181111 at 1/500. Cells were fixed with 4% paraformaldehyde and permeabilized with 0.1% Triton X-100. ab150077, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/500) was used as the secondary antibody. DAPI (blue) was used as the nuclear counterstain. ab7291, a mouse anti-tubulin (1/1000) and ab150120, an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/500) were also used.
Control 1 : primary antibody (1/500) and secondary antibody, ab150120, an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/500).
Control 2 : ab7291 (1/1000) and secondary antibody, ab150077, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/500).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human breast carcinoma tissue labeling FUBP1/FBP with unpurified ab181111 at a dilution of 1/500 followed by prediluted HRP Polymer for rabbit IgG. Counterstained with Hematoxylin.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
Intracellular flow cytometric analysis of2% paraformaldehyde-fixed Jurkat cells labeling FUBP1/FBP with unpurified ab181111 at a dilution of 1/90 (pink), compared to a rabbit monoclonal IgG isotype control (green), followed by goat anti rabbit IgG (FITC) secondary antibody at a dilution of 1/150.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
Immunocytochemistry/Immunofluorescent analysis of 4% paraformaldehyde-fixed HepG2 cells labeling FUBP1/FBP with unpurified ab181111 at 1/500 dilution (red) followed by Alexa Fluor® 555-conjugated goat anti rabbit IgG secondary antibody at 1/200 dilution. Counter stained with Dapi (blue).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human breast carcinoma tissue labelling FUBP1/FBP with purified ab181111 at 1/500. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9. ab97051, a HRP-conjugated goat anti-rabbit IgG (H+L) was used as the secondary antibody (1/500). Negative control using PBS instead of primary antibody. Counterstained with hematoxylin.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human pancreas tissue labeling FUBP1/FBP with unpurified ab181111 at a dilution of 1/500 followed by prediluted HRP Polymer for rabbit IgG. Counterstained with Hematoxylin.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
Intracellular Flow Cytometry analysis of Jurkat cells labelling FUBP1 / FBP with purified ab181111 at 1/60 (red). Cells were fixed with 80% methanol. A FITC-conjugated goat anti-rabbit IgG (1/150) was used as the secondary antibody. Black - Isotype control, rabbit monoclonal IgG. Blue - Unlabelled control, cells without incubation with primary and secondary antibodies.
- WB
Lab
Western blot - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-FUBP1/FBP antibody [EPR12327] (ab181111) at 1/5000 dilution
All lanes:
HepG2 cell lysate at 20 µg
Secondary
All lanes:
Peroxidase-conjugated goat anti-rabbit IgG, (H+L) at 1/1000 dilution
Predicted band size: 68 kDa
Observed band size: 74 kDa
false
- WB
Lab
Western blot - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-FUBP1/FBP antibody [EPR12327] (ab181111) at 1/20000 dilution
Lane 1:
Jurkat cell lysate at 20 µg
Lane 2:
HeLa cell lysate at 20 µg
Lane 3:
Raji cell lysate at 20 µg
Lane 4:
K562 cell lysate at 20 µg
Secondary
All lanes:
Peroxidase-conjugated goat anti-rabbit IgG, (H+L) at 1/1000 dilution
Predicted band size: 68 kDa
Observed band size: 74 kDa
false
- WB
Lab
Western blot - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-FUBP1/FBP antibody [EPR12327] (ab181111) at 1/5000 dilution
All lanes:
Rat brain tissue lysate at 20 µg
Secondary
All lanes:
Peroxidase-conjugated goat anti-rabbit IgG, (H+L) at 1/1000 dilution
Predicted band size: 68 kDa
Observed band size: 74 kDa
false
- WB
Lab
Western blot - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-FUBP1/FBP antibody [EPR12327] (ab181111) at 1/2000 dilution
Lane 1:
Mouse brain tissue lysate at 20 µg
Lane 2:
Mouse spleen tissue lysate at 20 µg
Secondary
All lanes:
Peroxidase-conjugated goat anti-rabbit IgG, (H+L) at 1/1000 dilution
Predicted band size: 132 kDa,68 kDa
Observed band size: 74 kDa
false
- WB
Supplier Data
Western blot - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
All lanes:
Western blot - Anti-FUBP1/FBP antibody [EPR12327] (ab181111) at 1/5000 dilution
All lanes:
Jurkat cell lysate at 20 µg
Secondary
All lanes:
Goat anti-rabbit IgG, (H+L), Peroxidase conjugate at 1/1000 dilution
Predicted band size: 68 kDa
Observed band size: 74 kDa
false
- WB
Supplier Data
Western blot - Anti-FUBP1/FBP antibody [EPR12327] (AB181111)
All lanes:
Western blot - Anti-FUBP1/FBP antibody [EPR12327] (ab181111) at 1/20000 dilution
Lane 1:
HeLa cell lysate at 20 µg
Lane 2:
HepG2 cell lysate at 20 µg
Secondary
All lanes:
Goat anti-rabbit IgG, (H+L), Peroxidase conjugate at 1/1000 dilution
Predicted band size: 68 kDa
Observed band size: 74 kDa
false
Reactivity data
Product details
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 duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
FUBP1 influences cellular proliferation and differentiation. It does not form part of a larger complex but interacts with different molecules to exert its function. The protein acts as an activator of transcription fostering interaction with RNA polymerase II and other factors to elevate gene expression. FUBP1's activity helps in controlling the cell cycle aiding in the switch between proliferation and cell growth arrest as needed.
Pathways
FUBP1 participates significantly in the c-Myc regulatory and p53 signaling pathways. In the context of the c-Myc pathway FUBP1 boosts the expression of c-Myc by stabilizing its mRNA a process also influenced by the U2 auxiliary factor (U2AF65). In the p53 signaling pathway FUBP1 indirectly influences p53's role in apoptosis and cellular stress responses as its regulatory balance shifts critical cellular processes depending on external and internal cues.
Product protocols
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Target data
Publications (13)
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PeerJ 11:e15917 PubMed37637163
2023
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Communications biology 5:672 PubMed35798971
2022
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Journal of bone oncology 31:100392 PubMed34712553
2021
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Journal of immunology research 2021:9994004 PubMed33987449
2021
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Frontiers in oncology 11:602712 PubMed33791202
2021
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Communications biology 3:545 PubMed33005010
2020
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Cells 9: PubMed32481602
2020
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Chinese medical journal 133:1211-1220 PubMed32433053
2020
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Cancer biology & therapy 21:213-222 PubMed31651209
2019
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Cell reports 28:3435-3449.e5 PubMed31553912
2019
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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