重组Anti-Rab4抗体[EPR3042] - Early Endosome Marker
Anti-Rab4 antibody [EPR3042] - Early Endosome Marker
- RabMAb
- Recombinant
- KO Validated
- Lab Essentials
- 了解详情
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(6 Publications)
Rabbit Recombinant Monoclonal Rab4 antibody. Early Endosome marker. Suitable for WB, ICC/IF and reacts with Mouse, Rat, Human samples. Cited in 6 publications.
查看别名
RAB4, RAB4A, Ras-related protein Rab-4A
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-Rab4 antibody [EPR3042] - Early Endosome Marker (AB108974)
Immunofluorescent staining of Rab4 in HeLa cells, using unpurified ab108974 at a 1/100 dilution.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Rab4 antibody [EPR3042] - Early Endosome Marker (AB108974)
Immunocytochemistry/ Immunofluorescence analysis of MCF7 (Human breast adenocarcinoma epithelial cell) cells labeling Rab4 with purified ab108974 at 1 : 100 dilution (8.8μg/ml). Cells were fixed in 4% Paraformaldehyde and permeabilized with 0.1% tritonX-100. Cells were counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) 1 : 200 (2.5 μg/ml). ab150077 Goat anti rabbit IgG(Alexa Fluor® 488) was used as the secondary antibody at 1 : 1000 dilution. DAPI nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.
- WB
Lab
Western blot - Anti-Rab4 antibody [EPR3042] - Early Endosome Marker (AB108974)
Lane 1 : Wild-type HAP1 cell lysate (20 μg)
Lane 2 : Rab4 knockout HAP1 cell lysate (20 μg)
Lane 3 : HeLa cell lysate (20 μg)
Lane 4 : Human fetal brain cell lysate (20 μg)
Lanes 1 - 4 : Merged signal (red and green). Green - ab108974 observed at 24 kDa. Red - loading control, ab8245, observed at 37 kDa.
Unpurified ab108974 was shown to recognize Rab4 when Rab4 knockout samples were used, along with additional cross-reactive bands. Wild-type and Rab4 knockout samples were subjected to SDS-PAGE. Unpurified ab108974 and ab8245 (loading control to GAPDH) were both diluted 1/2000 and incubated overnight at 4°C. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1/10 000 dilution for 1 h at room temperature before imaging.
All lanes:
Western blot - Anti-Rab4 antibody [EPR3042] - Early Endosome Marker (ab108974)
Predicted band size: 24 kDa
false
- WB
Lab
Western blot - Anti-Rab4 antibody [EPR3042] - Early Endosome Marker (AB108974)
Lanes 1- 2 : Merged signal (red and green). Green - ab108974 observed at 24 kDa. Red - Anti-GAPDH antibody [6C5] - Loading Control (ab8245) observed at 37 kDa.
ab108974 was shown to react with Rab4 in wild-type HeLa cells in western blot. Loss of signal was observed when knockout cell line ab264781 (knockout cell lysate ab257624) was used. Wild-type HeLa and RAB4A knockout HeLa cell lysates were subjected to SDS-PAGE. ab108974 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) overnight at 4°C at a 1 in 1000 Dilution and a 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye®800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye®680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-Rab4 antibody [EPR3042] - Early Endosome Marker (ab108974) at 1/1000 dilution
Lane 1:
Wild-type HeLa cell lysate at 40 µg
Lane 2:
RAB4A knockout HeLa cell lysate at 40 µg
Predicted band size: 152 kDa,24 kDa,41 kDa
Observed band size: 24 kDa,44 kDa,80 kDa
false
- WB
Lab
Western blot - Anti-Rab4 antibody [EPR3042] - Early Endosome Marker (AB108974)
Blocking and diluting buffer : 5% NFDM/TBST
All lanes:
Western blot - Anti-Rab4 antibody [EPR3042] - Early Endosome Marker (ab108974) at 1/2000 dilution
Lane 1:
MCF7 (Human breast adenocarcinoma epithelial cell) whole cell lysates at 20 µg
Lane 2:
PC-12 (Rat adrenal gland pheochromocytoma) whole cell lysates at 20 µg
Lane 3:
Neuro-2a (Mouse neuroblastoma neuroblast) whole cell lysates at 20 µg
Lane 4:
Mouse brain lysates at 20 µg
Lane 5:
Rat brain lysates 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 1/20000 dilution
Predicted band size: 24 kDa
Observed band size: 25 kDa
false
- WB
Unknown
Western blot - Anti-Rab4 antibody [EPR3042] - Early Endosome Marker (AB108974)
All lanes:
Western blot - Anti-Rab4 antibody [EPR3042] - Early Endosome Marker (ab108974) at 1/2000 dilution
Lane 1:
MCF7 cell lysates at 10 µg
Lane 2:
PC12 cell lysates at 10 µg
Lane 3:
Fetal brain cell lysates at 10 µg
Secondary
All lanes:
HRP labelled goat anti-rabbit at 1/2000 dilution
Predicted band size: 24 kDa
Observed band size: 25 kDa
false
不同偶联物与剂型 (2)
-
HRP Anti-Rab4 antibody [EPR3042] - Early Endosome Marker
-
Anti-Rab4 antibody [EPR3042] - BSA and Azide free
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
Rab4 coordinates the trafficking of cargo between endosomes and the plasma membrane. It usually forms part of a protein complex that governs the recycling pathway of internalized membrane proteins and lipids. Rab4 modulates various cellular processes by impacting the rapid recycling of receptors receptors often return to the cell surface in response to Rab4 regulation. This action is important for maintaining cellular homeostasis and efficient signal transduction serving as a checkpoint for receptor-mediated events.
Pathways
The protein plays significant roles in the endocytic recycling pathway and the insulin signaling pathway. Rab4's activity influences the trafficking cycle often interacting with other proteins such as Rab11 and Rab5 to ensure efficient cargo movement within cells. By facilitating swift endosome recycling Rab4 has a direct impact on intracellular signaling and trafficking pathways supporting a range of cellular activities. This concerted interaction accentuates its importance in managing endosomal traffic and maintaining cellular connectivity.
产品实验方案
- Visit the General protocols
- Visit the Troubleshooting
靶点信息
文献 (6)
Recent publications for all applications. Explore the full list and refine your search
Nature communications 15:2598 PubMed38519468
2024
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EMBO reports 23:e53373 PubMed34994492
2022
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Biochemistry 58:2628-2641 PubMed30896156
2019
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Nature methods 15:909-912 PubMed30377371
2018
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The Journal of biological chemistry 293:3421-3435 PubMed29317492
2018
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Neuroscience 361:93-107 PubMed28818525
2017
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