重组Anti-DRIP130抗体[EPR17418]
Anti-DRIP130 antibody [EPR17418]
- RabMAb
- Recombinant
- 了解详情
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(5 Publications)
Rabbit Recombinant Monoclonal DRIP130 antibody. Suitable for WB, ICC/IF, IHC-P and reacts with Mouse, Rat, Human samples. Cited in 5 publications.
查看别名
ARC130, CRSP3, DRIP130, KIAA1216, SUR2, MED23, Mediator of RNA polymerase II transcription subunit 23, Activator-recruited cofactor 130 kDa component, Cofactor required for Sp1 transcriptional activation subunit 3, Mediator complex subunit 23, Protein sur-2 homolog, Transcriptional coactivator CRSP130, Vitamin D3 receptor-interacting protein complex 130 kDa component, CRSP complex subunit 3, hSur-2
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-DRIP130 antibody [EPR17418] (AB200351)
Immunohistochemical analysis of paraffin-embedded Human breast carcinoma tissue labeling DRIP130 with ab200351 at 1/250 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Nuclear staining on Human breast carcinoma tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-DRIP130 antibody [EPR17418] (AB200351)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized MCF7 (Human breast adenocarcinoma cell line) cells labeling DRIP130 with ab200351 at 1/1000 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Confocal image showing nuclear staining on MCF7 cell line. The nuclear counter stain is DAPI (blue). Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows :
-ve control 1 : ab200351 at 1/1000 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2 : ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/500 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-DRIP130 antibody [EPR17418] (AB200351)
Immunohistochemical analysis of paraffin-embedded rat kidney tissue labeling DRIP130 with ab200351 at 1/250 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Nuclear staining on rat kidney tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- WB
Supplier Data
Western blot - Anti-DRIP130 antibody [EPR17418] (AB200351)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-DRIP130 antibody [EPR17418] (ab200351) at 1/10000 dilution
Lane 1:
MCF7 (Human breast adenocarcinoma cell line) whole cell lysate at 10 µg
Lane 2:
HeLa (Human epithelial cells from cervix adenocarcinoma) whole cell lysate at 10 µg
Lane 3:
HEK-293 (Human epithelial cells from embryonic kidney) whole cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 156 kDa
Observed band size: 130 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-DRIP130 antibody [EPR17418] (AB200351)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-DRIP130 antibody [EPR17418] (ab200351) at 1/1000 dilution
Lane 1:
Human fetal brain lysate at 10 µg
Lane 2:
Human fetal kidney lysate at 10 µg
Secondary
All lanes:
Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 156 kDa
Observed band size: 130 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-DRIP130 antibody [EPR17418] (AB200351)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-DRIP130 antibody [EPR17418] (ab200351) at 1/1000 dilution
Lane 1:
Mouse kidney lysate at 10 µg
Lane 2:
Mouse spleen lysate at 10 µg
Lane 3:
C6 (Rat glial tumor cells) whole cell lysate at 10 µg
Lane 4:
RAW 264.7 (Mouse macrophage cells transformed with Abelson murine leukemia virus ) whole cell lysate at 10 µg
Lane 5:
PC-12 (Rat adrenal gland pheochromocytoma) whole cell lysate at 10 µg
Lane 6:
NIH/3T3 (Mouse embyro fibroblast cells ) whole cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 156 kDa
Observed band size: 130 kDa
false
Exposure time: 15s
- WB
Supplier Data
Western blot - Anti-DRIP130 antibody [EPR17418] (AB200351)
The observed MW is consistent with what has been described in the literature (PMID : 12242338).
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-DRIP130 antibody [EPR17418] (ab200351) at 1/1000 dilution
All lanes:
Rat kidney lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 156 kDa
Observed band size: 130 kDa
false
Exposure time: 3min
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.
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
DRIP130 integrates signals from activators and repressors to facilitate transcription regulation. It is a part of the larger Mediator complex which is essential for conveying instructions from transcription factors to RNA polymerase II. By acting at promoters DRIP130 helps modulate gene expression impacting processes like cell growth and differentiation. Its function within this multi-subunit complex emphasizes its importance in cellular communication and transcriptional regulation.
Pathways
DRIP130 contributes to the MAPK/ERK signaling pathway and the Wnt signaling pathway. Within these pathways it interacts with proteins such as MAPK and β-catenin to influence cell cycle progression and cellular responses. These pathways are critical for controlling growth and maintaining cellular functions indicating DRIP130's vital role in pathway integration and cellular homeostasis.
产品实验方案
- Visit the General protocols
- Visit the Troubleshooting
靶点信息
文献 (5)
Recent publications for all applications. Explore the full list and refine your search
Cell discovery 11:69 PubMed40825935
2025
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Unspecified reactive species
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 50:1224-1236 PubMed40114018
2025
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Unspecified reactive species
iScience 26:107143 PubMed37456852
2023
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Nucleic acids research 51:2137-2150 PubMed36718943
2023
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Unspecified reactive species
Autophagy 17:3592-3606 PubMed33629929
2021
Applications
Unspecified application
Species
Unspecified reactive species
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