重组Anti-ATP6V1B1 + ATP6V1B2抗体[EPR16401]
Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401]
- RabMAb
- Recombinant
- 了解详情
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(16 Publications)
Rabbit Recombinant Monoclonal ATP6V1B1 antibody. Suitable for WB, ICC/IF, IHC-P and reacts with Mouse, Human, Rat samples. Cited in 16 publications.
查看别名
ATP6B1, VATB, VPP3, ATP6V1B1, V-ATPase subunit B 1, Endomembrane proton pump 58 kDa subunit, Vacuolar proton pump subunit B 1
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] (AB200839)
Immunofluorescent analysis of 100% methanol-fixed, 0.1% Triton X-100 permeabilized HEK293 (Human embryonic kidney) cells labeling ATP6V1B1 + ATP6V1B2 with ab200839 at 1/250 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Cytoplasmic staining on HEK293 cell line was observed. 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 : ab200839 at 1/250 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.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] (AB200839)
Immunofluorescent analysis of 100% methanol-fixed, 0.1% Triton X-100 permeabilized JAR (Human placenta choriocarcinoma cell line) cells labeling ATP6V1B1 + ATP6V1B2 with ab200839 at 1/250 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Cytoplasmic staining on JAR cell line was observed. 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 : ab200839 at 1/250 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-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] (AB200839)
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling ATP6V1B1 + ATP6V1B2 with ab200839 at 1/5000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Cytoplasmic staining on Human 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.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] (AB200839)
Immunohistochemical analysis of paraffin-embedded Human cardiac muscle tissue labeling ATP6V1B1 + ATP6V1B2 with ab200839 at 1/5000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Human cardiac muscle tissue represents a negative control for ATP6V1B1 + ATP6V1B2. 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.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] (AB200839)
Immunohistochemical analysis of paraffin-embedded Mouse kidney tissue labeling ATP6V1B1 + ATP6V1B2 with ab200839 at 1/5000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Cytoplasmic staining on mouse 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.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] (AB200839)
Immunohistochemical analysis of paraffin-embedded Rat kidney tissue labeling ATP6V1B1 + ATP6V1B2 with ab200839 at 1/5000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Cytoplasmic 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-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] (AB200839)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] (ab200839) at 1/1000 dilution
Lane 1:
JAR (Human placenta choriocarcinoma cell line) cell lysate at 10 µg
Lane 2:
JAR (Human placenta choriocarcinoma cell line) cell lysate at 10 µg with immunizing peptide
Lane 3:
JAR (Human placenta choriocarcinoma cell line) cell lysate at 10 µg with ATP6V1B2 peptide
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 57 kDa
Observed band size: 57 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] (AB200839)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] (ab200839) at 1/5000 dilution
All lanes:
JAR (Human placenta choriocarcinoma cell line) cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 57 kDa
Observed band size: 57 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] (AB200839)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] (ab200839) at 1/1000 dilution
Lane 1:
Mouse brain lysate at 10 µg
Lane 2:
Mouse kidney lysate at 10 µg
Lane 3:
Rat kidney lysate at 10 µg
Lane 4:
RAW 264.7 (Mouse macrophage cells transformed with Abelson murine leukemia virus) cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 57 kDa
Observed band size: 57 kDa
false
Exposure time: 3min
不同偶联物与剂型 (2)
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Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401] - BSA and Azide free
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-ATP6V1B1 + ATP6V1B2 antibody [EPR16401]
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
ATP6V1B1 and ATP6V1B2 participate in acidification of intracellular environments a fundamental process for cellular homeostasis and function. They are integral components of the V-ATPase complex which actively transports protons into lysosomes endosomes and other vesicles generating acidic conditions essential for protein degradation vesicular trafficking and hormone activation. This acidification is also important for maintaining the optimal pH necessary for various enzymatic activities within organelles.
Pathways
These subunits play an important role in the regulation of the mTOR signaling pathway and endocytosis pathway both critical for cell growth proliferation and nutrient sensing. The activity of V-ATPase influences these pathways by affecting pH-dependent processes required for receptor-mediated endocytosis and nutrient availability. ATP6V1B1 and ATP6V1B2 interact with other V-ATPase subunits such as ATP6V1A and ATP6V1C to modulate their function in these pathways.
产品实验方案
- Visit the General protocols
- Visit the Troubleshooting
靶点信息
其他靶点
文献 (16)
Recent publications for all applications. Explore the full list and refine your search
Nature cell biology 26:2020-2034 PubMed39528700
2024
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Cell reports 42:113529 PubMed38060380
2023
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Nature communications 14:7783 PubMed38012166
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Journal of virology 97:e0133823 PubMed38009916
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The Journal of cell biology 222: PubMed36880731
2023
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Nature metabolism 5:111-128 PubMed36658400
2023
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Life science alliance 6: PubMed36650057
2023
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eLife 11: PubMed35119364
2022
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Nature communications 13:571 PubMed35091558
2022
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Bone research 9:36 PubMed34334792
2021
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