重组Anti-SENP1抗体[EPR3844]
Anti-SENP1 antibody [EPR3844]
- RabMAb
- Recombinant
- 20ul selling size
- 了解详情
5
(7 Reviews)
|
(55 Publications)
Rabbit Recombinant Monoclonal SENP1 antibody. Suitable for IHC-P, WB, ICC/IF, Flow Cyt (Intra) and reacts with Human samples. Cited in 55 publications.
查看别名
Sentrin-specific protease 1, Sentrin/SUMO-specific protease SENP1, SENP1
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SENP1 antibody [EPR3844] (AB108981)
Immunohistochemical staining of paraffin embedded human testis with purified ab108981 at a working dilution of 1/300. The secondary antibody used is HRP goat anti-rabbit IgG H&L (ab97051) at 1/500. The sample is counter-stained with hematoxylin. Antigen retrieval was perfomed using Tris-EDTA buffer, pH 9.0. PBS was used instead of the primary antibody as the negative control, and is shown in the inset.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-SENP1 antibody [EPR3844] (AB108981)
Immunofluorescence staining of Jurkat cells with purified ab108981 at a working dilution of 1/100, counter-stained with DAPI. The secondary antibody was Alexa Fluor® 488 goat anti-rabbit (ab150077), used at a dilution of 1/1000. ab7291, a mouse anti-tubulin antibody (1/1000), was used to stain tubulin along with ab150120 (Alexa Fluor® 594 goat anti-mouse, 1/1000), shown in the top right hand panel. The cells were fixed in 4% PFA and permeabilized using 0.1% Triton X 100. The negative controls are shown in bottom middle and right hand panels - for negative control 1, purified ab108981 was used at a dilution of 1/500 followed by an Alexa Fluor® 594 goat anti-mouse antibody (ab150120) at a dilution of 1/500. For negative control 2, ab7291 (mouse anti-tubulin) was used at a dilution of 1/500 followed by an Alexa Fluor® 488 goat anti-rabbit antibody (ab150077) at a dilution of 1/400.
- ICC/IF
AbReview29250****
Immunocytochemistry/ Immunofluorescence - Anti-SENP1 antibody [EPR3844] (AB108981)
Unpurified ab108981 (1/500) staining SENP1 in HeLa cells (green). Cells were fixed in paraformaldehyde, permeabilised with 0.5% Triton X-100/PBS and counterstained with DAPI in order to highlight the nucleus (red). For further experimental details please refer to Abreview.
Image courtesy of an Abreview submitted by Dr. Kirk McManus, Univ. of Manitoba/Cancer Care MICB, Canada
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-SENP1 antibody [EPR3844] (AB108981)
Intracellular Flow Cytometry analysis of HeLa cells labelling SENP1 with purified ab108981 at a dilution of 1/20 (red). Cells were fixed with 4% paraformaldehyde and permeabilized with 90% methanol. An Alexa Flour® 488-conjugated goat anti-rabbit IgG (1/2000) 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-SENP1 antibody [EPR3844] (AB108981)
Blocking buffer : 5% NFDM/TBST
Dilution buffer : 5% NFDM/TBST
All lanes:
Western blot - Anti-SENP1 antibody [EPR3844] (ab108981) at 1/20000 dilution
All lanes:
Daudi cell lysate at 10 µg
Secondary
All lanes:
HRP goat anti-rabbit IgG (H+L) at 1/20000 dilution
Predicted band size: 73 kDa
Observed band size: 73 kDa
false
- WB
Lab
Western blot - Anti-SENP1 antibody [EPR3844] (AB108981)
Blocking buffer : 5% NFDM/TBST
Dilution buffer : 5% NFDM/TBST
All lanes:
Western blot - Anti-SENP1 antibody [EPR3844] (ab108981) at 1/20000 dilution
All lanes:
U87-MG cell lysate at 10 µg
Secondary
All lanes:
HRP goat anti-rabbit IgG (H+L) at 1/20000 dilution
Predicted band size: 73 kDa
Observed band size: 73 kDa
false
- WB
AbReview48238****
Western blot - Anti-SENP1 antibody [EPR3844] (AB108981)
Blocked with 3% milk for 1 hour at 25°C.
Incubated with the primary antibody for 18 hours at 4°C.
All lanes:
Western blot - Anti-SENP1 antibody [EPR3844] (ab108981) at 1/1000 dilution
Lane 1:
COS-1 cell lysate at 20000 Cells
Lane 2:
COS-1 cell lysate transfected with SENP1 at 20000 Cells
Lane 3:
COS-1 cell lysate transfected with SENP1 mutant at 20000 Cells
Secondary
All lanes:
HRP-conjugated donkey anti-rabbit IgG polyclonal at 1/10000 dilution
Predicted band size: 73 kDa
Observed band size: 75 kDa
true
Exposure time: 6min
This image is courtesy of an Abreview submitted by Ragnhild Eskeland
- WB
Unknown
Western blot - Anti-SENP1 antibody [EPR3844] (AB108981)
All lanes:
Western blot - Anti-SENP1 antibody [EPR3844] (ab108981) at 1/1000 dilution
Lane 1:
HeLa cell lysates at 10 µg
Lane 2:
HUVEC cell lysates at 10 µg
Lane 3:
Jurkat cell lysates at 10 µg
Lane 4:
Daudi cell lysates at 10 µg
Lane 5:
U87-MG cell lysates at 10 µg
Secondary
All lanes:
Standard HRP labelled goat anti-rabbit at 1/2000 dilution
Predicted band size: 73 kDa
false
不同偶联物与剂型 (2)
-
HRP Anti-SENP1 antibody [EPR3844]
-
Anti-SENP1 antibody [EPR3844] - BSA and Azide free
反应性数据
产品详情
Species reactivity
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species.
Please contact us for more information.
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.
性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存时间
推荐的短期储存条件
推荐的长期储存条件
分装信息
储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
SENP1 contributes to cellular homeostasis by modifying and controlling protein interactions and functions. This enzyme facilitates the recycling of SUMO proteins and affects transcription factors such as HIF1α which are vital for cellular response to hypoxia. SENP1 interacts closely with SUMO E3 ligases in complexes coordinating the addition or removal of SUMO groups from target proteins. Its activity is essential for maintaining the balance between protein sumoylation and desumoylation which impacts numerous cellular processes including cell cycle progression and stress response.
Pathways
SENP1 modulates key regulatory pathways related to its sumoylation mechanism. Major pathways where SENP1 plays a role include the HIF-1 signaling pathway where it affects the stability and activity of HIF1α under low oxygen conditions and the p53 signaling pathway influencing cell cycle and apoptosis. SENP1's interactivity with proteins like Ubc9 a SUMO-conjugating enzyme and PIAS3 a SUMO E3 ligase indicates its broad involvement and regulation within these pathways emphasizing its impact on maintaining cellular function and adaptation.
产品实验方案
- Visit the General protocols
- Visit the Troubleshooting
靶点信息
文献 (55)
Recent publications for all applications. Explore the full list and refine your search
Nature communications 16:7308 PubMed40774970
2025
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International journal of molecular medicine 56: PubMed40682835
2025
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Nature communications 15:10805 PubMed39737943
2024
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Cell communication and signaling : CCS 22:465 PubMed39350261
2024
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Clinical and translational medicine 14:e1753 PubMed38967349
2024
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Cellular oncology (Dordrecht, Netherlands) 48:67-81 PubMed38954215
2024
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Nature communications 14:5688 PubMed37709794
2023
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The Journal of biological chemistry 299:105062 PubMed37468105
2023
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Biomedicines 11: PubMed36979893
2023
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Nature communications 13:7153 PubMed36414671
2022
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Abcam Product Promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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