Anti-SENP1 抗体 [EPR3844]
Anti-SENP1 antibody [EPR3844]
- RabMAb
- Recombinant
- 詳細を見る
5
(7 Reviews)
|
(43 Publications)
Rabbit Recombinant Monoclonal SENP1 antibody. Suitable for IHC-P, WB, ICC/IF, Flow Cyt (Intra) and reacts with Human samples. Cited in 43 publications.
別名を表示する
Sentrin-specific protease 1, Sentrin/SUMO-specific protease SENP1, SENP1
- 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
- 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.
- 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
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
- 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.
- 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
- 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
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
関連する標識済み抗体及び組成の異なる製品 (2)
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HRP Anti-SENP1 antibody [EPR3844]
-
Anti-SENP1 antibody [EPR3844] - BSA and Azide free
Reactivity data
製品の詳細
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.
出荷温度及び保存条件
製品の状態
精製方法
バッファー組成
出荷温度
短期保存期間
短期保存温度
長期保存温度
分注に関する情報
保管に関する情報
補足情報
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.
製品プロトコール
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ターゲットの情報
文献 (43)
Recent publications for all applications. Explore the full list and refine your search
Nature communications 14:5688 PubMed37709794
2023
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Nature communications 13:7153 PubMed36414671
2022
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Oncogenesis 11:65 PubMed36284084
2022
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Oxidative medicine and cellular longevity 2022:8002566 PubMed35707278
2022
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International journal of biological sciences 18:2186-2201 PubMed35342335
2022
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Frontiers in cell and developmental biology 9:789348 PubMed35186948
2022
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Cell death & disease 12:1067 PubMed34753901
2021
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Journal of cell science 134: PubMed34313310
2021
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The FEBS journal 288:6447-6464 PubMed34089566
2021
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Cell death & disease 12:341 PubMed33795649
2021
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