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AB73404

Anti-ATP6V1B2抗体

Anti-ATP6V1B2 antibody

5

(1 Review)

|

(29 Publications)

Rabbit Polyclonal ATP6V1B2 antibody. Suitable for IHC-P, IP, WB, ICC/IF and reacts with Human, Mouse, Rat samples. Cited in 29 publications.

查看别名

ATP6B2, VPP3, ATP6V1B2, V-ATPase subunit B 2, Endomembrane proton pump 58 kDa subunit, HO57, Vacuolar proton pump subunit B 2

6 Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ATP6V1B2 antibody (AB73404)
  • IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ATP6V1B2 antibody (AB73404)

IHC image of ATP6V1B2 staining in human hippocampus formalin fixed paraffin embedded tissue section, performed on a Leica BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab73404, 0.5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Immunocytochemistry/ Immunofluorescence - Anti-ATP6V1B2 antibody (AB73404)
  • ICC/IF

Unknown

Immunocytochemistry/ Immunofluorescence - Anti-ATP6V1B2 antibody (AB73404)

ICC/IF image of ab73404 stained PC12 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab73404, 5µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM. This antibody also gave a positive result in 4% PFA fixed (10 min) PC12 cells at 5µg/ml.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ATP6V1B2 antibody (AB73404)
  • IHC-P

AbReview34387****

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ATP6V1B2 antibody (AB73404)

ab73404 staining RAt incisor tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with formaldehyde and blocked with 2.5% serum for 30 minutes at 22°C. Samples were incubated with primary antibody (1/1000 in 1% BSA/ 0.5% Triton X-100 in PBS) for 16 hours at 4°C. An undiluted peroxidase-conjugated Goat anti-rabbit IgG polyclonal was used as the secondary antibody.

This image is courtesy of an anonymous Abreview

Immunoprecipitation - Anti-ATP6V1B2 antibody (AB73404)
  • IP

Unknown

Immunoprecipitation - Anti-ATP6V1B2 antibody (AB73404)

ATP6V1B2 was immunoprecipitated using 0.5mg Mouse Testis tissue lysate, 5µg of Rabbit polyclonal to ATP6V1B2 and 50µl of protein G magnetic beads (+). No antibody was added to the control (-).
The antibody was incubated under agitation with Protein G beads for 10min, Mouse Testis tissue lysate lysate diluted in RIPA buffer was added to each sample and incubated for a further 10min under agitation.
Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab73404.
Secondary : Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697).
Band : 57kDa; ATP6V1B2

All lanes:

Immunoprecipitation - Anti-ATP6V1B2 antibody (ab73404)

Predicted band size: 57 kDa

false

Western blot - Anti-ATP6V1B2 antibody (AB73404)
  • WB

Project

Western blot - Anti-ATP6V1B2 antibody (AB73404)

Lanes 1-6 were blocked with 5% BSA, Lanes 7-12 were blocked with 3% milk. Abcam recommends using milk as the blocking agent. Abcam welcomes customer feedback and would appreciate any comments regarding this product and the data presented above.

All lanes:

Western blot - Anti-ATP6V1B2 antibody (ab73404) at 1 µg/mL

Lanes 1 and 7:

Hippocampus (Mouse) Tissue Lysate at 10 µg

Lanes 2 and 8:

Kidney (Mouse) Tissue Lysate at 10 µg

Lanes 3 and 9:

Testis (Mouse) Tissue Lysate at 10 µg

Lanes 4 and 10:

Human testis tissue lysate - total protein (<a href='/products/unavailable/human-testis-tissue-lysate-total-protein-ab30257'>ab30257</a>) at 10 µg

Lanes 5 and 11:

Human kidney tissue lysate - total protein (<a href='/products/unavailable/human-kidney-tissue-lysate-total-protein-ab30203'>ab30203</a>) at 10 µg

Lanes 6 and 12:

Rat Hippocampus Tissue Lysate at 10 µg

Secondary

All lanes:

Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) (ab65484) at 1/3000 dilution

Predicted band size: 57 kDa

Observed band size: 37 kDa,57 kDa

false

Exposure time: 30s

Western blot - Anti-ATP6V1B2 antibody (AB73404)
  • WB

CiteAb

Western blot - Anti-ATP6V1B2 antibody (AB73404)

ATP6V1B2 western blot using anti-ATP6V1B2 antibody ab73404. Publication image and figure legend from Sun, J., Li, Y., et al., 2022, Aging Cell, PubMed 34905649.

ab73404 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab73404 please see the product overview.

GDF11 decreases lysosomal function. (a) AML-12 cells transient expressing GFP-LC3 were cultured for 48 h in presence of GDF11 (100 ng/ml). After staining with LysoTracker Red DND-99, cells were examined by confocal microscopy. Immunofluorescence confocal microscopy showing colocalization between LC3 puncta and LysoTracker Red with or without GDF11 (original magnification, 400×). (b) Quantification of the fluorescence intensity LC3 overlapping with Lysotracker signal normalized to vehicle controls. (c) Representative images of self-quenched DQ-BSA in AML-12 cells (original magnification, 400×). (d) Quantification of the fluorescence intensity of DQ-BSA normalized to vehicle controls. (e) Western blot analysis of m-cathepsin B, ATP6V1a, and ATP6V1b2 protein expression. (f) Densitometry analysis of the m-cathepsin B, ATP6V1a, and ATP6V1b2. The experiment was performed in triplicate with similar results. The data are shown as mean ± SD, *p < 0.05 compared to the vehicle group

false

关键信息

宿主种属

Rabbit

克隆

Polyclonal

亚型

IgG

不含载体蛋白

No

反应种属

Mouse, Rat, Human

应用

IHC-P, ICC/IF, WB, IP

applications

免疫原

The exact immunogen used to generate this antibody is proprietary information.

反应性数据

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性能和储存信息

形式
Liquid
纯化工艺
Affinity purification Immunogen
存储溶液
pH: 7.4 Preservative: 0.02% Sodium azide Constituents: PBS, 1% BSA
运输条件
Blue Ice
推荐的短期储存时间
1-2 weeks
推荐的短期储存条件
+4°C
推荐的长期储存条件
-20°C
分装信息
Upon delivery aliquot
储存信息
Avoid freeze / thaw cycle

补充信息

This supplementary information is collated from multiple sources and compiled automatically.

ATP6V1B2 also known as V-type proton ATPase subunit B2 is an essential component of the vacuolar ATPase (V-ATPase) complex. It weighs approximately 56 kDa. This protein is responsible for the hydrolysis of ATP supplying energy for proton translocation across membranes. ATP6V1B2 is heavily expressed in various tissues including the brain and kidney. As part of the V1 domain of the V-ATPase it plays an important role in regulating intracellular pH.
Biological function summary

ATP6V1B2 contributes to several key processes by enabling proton transport critical for organelle acidification. It is a component of the V-ATPase complex a multi-subunit complex important for the acidification of intracellular compartments. Organelle acidification affects processes like protein degradation neurotransmitter loading and receptor-mediated endocytosis. ATP6V1B2 specifically aids in the stabilization and assembly of the V-ATPase complex ensuring effective proton pumping activity in diverse cellular environments.

Pathways

ATP6V1B2 plays a significant role in both endocytic and autophagic pathways. The endocytic pathway integrates proteins such as clathrin and dynamin which are important for the internalization and recycling of membrane components. In autophagy ATP6V1B2 assists in the fusion of autophagosomes with lysosomes influencing cellular homeostasis and response to nutrient deprivation. These pathways are integral for maintaining cellular energy balance growth and survival.

ATP6V1B2 has associations with conditions such as dominant and recessive cutis laxa type II and Zimmermann-Laband syndrome. These diseases often display craniofacial abnormalities and variable connective tissue symptoms. Connections with proteins like ATP6V1A have been identified which also participate in similar disorders due to shared structural roles in maintaining proper V-ATPase complex function. Understanding these links can further research into targeted therapeutic strategies.

产品实验方案

For this product, it's our understanding that no specific protocols are required. You can visit:

靶点信息

Non-catalytic subunit of the V1 complex of vacuolar(H+)-ATPase (V-ATPase), a multisubunit enzyme composed of a peripheral complex (V1) that hydrolyzes ATP and a membrane integral complex (V0) that translocates protons (PubMed : 33065002). V-ATPase is responsible for acidifying and maintaining the pH of intracellular compartments and in some cell types, is targeted to the plasma membrane, where it is responsible for acidifying the extracellular environment (PubMed : 32001091). In renal intercalated cells, can partially compensate the lack of ATP6V1B1 and mediate secretion of protons (H+) into the urine under base-line conditions but not in conditions of acid load (By similarity).
See full target information ATP6V1B2

文献 (29)

Recent publications for all applications. Explore the full list and refine your search

The Journal of cell biology 224: PubMed40067150

2025

The deubiquitinase USP45 inhibits autophagy through actin regulation by Coronin 1B.

Applications

Unspecified application

Species

Unspecified reactive species

Yuchieh Jay Lin,Li-Ting Huang,Po-Yuan Ke,Guang-Chao Chen

iScience 28:111515 PubMed39758816

2025

TBC1D24 interacts with the v-ATPase and regulates intraorganellar pH in neurons.

Applications

Unspecified application

Species

Unspecified reactive species

Sara Pepe,Davide Aprile,Enrico Castroflorio,Antonella Marte,Simone Giubbolini,Samir Hopestone,Anna Parsons,Tânia Soares,Fabio Benfenati,Peter L Oliver,Anna Fassio

Nature 643:201-209 PubMed39695235

2024

Lithocholic acid binds TULP3 to activate sirtuins and AMPK to slow down ageing.

Applications

Unspecified application

Species

Unspecified reactive species

Qi Qu,Yan Chen,Yu Wang,Weiche Wang,Shating Long,Heng-Ye Yang,Jianfeng Wu,Mengqi Li,Xiao Tian,Xiaoyan Wei,Yan-Hui Liu,Shengrong Xu,Jinye Xiong,Chunyan Yang,Zhenhua Wu,Xi Huang,Changchuan Xie,Yaying Wu,Zheni Xu,Cixiong Zhang,Baoding Zhang,Jin-Wei Feng,Junjie Chen,Yuanji Feng,Huapan Fang,Liyun Lin,Z K Xie,Beibei Sun,Huayu Tian,Yong Yu,Hai-Long Piao,Xiao-Song Xie,Xianming Deng,Chen-Song Zhang,Sheng-Cai Lin

Andrology 13:1509-1529 PubMed39363435

2024

hACE2 upregulation and participation of macrophages and clear cells in the immune response of epididymis to SARS-CoV-2 in K18-hACE2 mice.

Applications

Unspecified application

Species

Unspecified reactive species

André Acácio Souza da Silva,Salmo Azambuja de Oliveira,Maria Agustina Battistone,Barry Thomas Hinton,Paulo Sérgio Cerri,Estela Sasso-Cerri

Acta physiologica (Oxford, England) 240:e14186 PubMed38837572

2024

ATP6V1A is required for synaptic rearrangements and plasticity in murine hippocampal neurons.

Applications

Unspecified application

Species

Unspecified reactive species

Alessandro Esposito,Sara Pepe,Maria Sabina Cerullo,Katia Cortese,Hanako Tsushima Semini,Silvia Giovedì,Renzo Guerrini,Fabio Benfenati,Antonio Falace,Anna Fassio

Frontiers in molecular neuroscience 16:1170313 PubMed37138705

2023

Peroxisomal defects in microglial cells induce a disease-associated microglial signature.

Applications

Unspecified application

Species

Unspecified reactive species

Quentin Raas,Ali Tawbeh,Mounia Tahri-Joutey,Catherine Gondcaille,Céline Keime,Romain Kaiser,Doriane Trompier,Boubker Nasser,Valerio Leoni,Emma Bellanger,Maud Boussand,Yannick Hamon,Alexandre Benani,Francesca Di Cara,Caroline Truntzer,Mustapha Cherkaoui-Malki,Pierre Andreoletti,Stéphane Savary

mSphere 8:e0052322 PubMed36719247

2023

The Lipid Raft-Associated Protein Stomatin Is Required for Accumulation of Dectin-1 in the Phagosomal Membrane and for Full Activity of Macrophages against Aspergillus fumigatus.

Applications

Unspecified application

Species

Unspecified reactive species

Marie Goldmann,Franziska Schmidt,Zoltán Cseresnyés,Thomas Orasch,Susanne Jahreis,Susann Hartung,Marc Thilo Figge,Marie von Lilienfeld-Toal,Thorsten Heinekamp,Axel A Brakhage

Nature communications 13:7578 PubMed36481721

2022

Intracellular galectin-3 is a lipopolysaccharide sensor that promotes glycolysis through mTORC1 activation.

Applications

Unspecified application

Species

Unspecified reactive species

Xing Chen,Chunyu Yu,Xinhua Liu,Beibei Liu,Xiaodi Wu,Jiajing Wu,Dong Yan,Lulu Han,Zifan Tang,Xinyi Yuan,Jianqiu Wang,Yue Wang,Shumeng Liu,Lin Shan,Yongfeng Shang

Nature metabolism 4:1369-1401 PubMed36217034

2022

The aldolase inhibitor aldometanib mimics glucose starvation to activate lysosomal AMPK.

Applications

Unspecified application

Species

Unspecified reactive species

Chen-Song Zhang,Mengqi Li,Yu Wang,Xiaoyang Li,Yue Zong,Shating Long,Mingliang Zhang,Jin-Wei Feng,Xiaoyan Wei,Yan-Hui Liu,Baoding Zhang,Jianfeng Wu,Cixiong Zhang,Wenhua Lian,Teng Ma,Xiao Tian,Qi Qu,Yaxin Yu,Jinye Xiong,Dong-Tai Liu,Zhenhua Wu,Mingxia Zhu,Changchuan Xie,Yaying Wu,Zheni Xu,Chunyan Yang,Junjie Chen,Guohong Huang,Qingxia He,Xi Huang,Lei Zhang,Xiufeng Sun,Qingfeng Liu,Abdul Ghafoor,Fu Gui,Kaili Zheng,Wen Wang,Zhi-Chao Wang,Yong Yu,Qingliang Zhao,Shu-Yong Lin,Zhi-Xin Wang,Hai-Long Piao,Xianming Deng,Sheng-Cai Lin

Frontiers in cell and developmental biology 9:743124 PubMed35252216

2022

HPS6 Regulates the Biogenesis of Weibel-Palade Body in Endothelial Cells Through Trafficking v-ATPase to Its Limiting Membrane.

Applications

Unspecified application

Species

Unspecified reactive species

Jiran Lu,Jing Ma,Zhenhua Hao,Wei Li
View all publications

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