Rabbit Recombinant Monoclonal VPS15 antibody. Suitable for WB and reacts with Mouse, Rat, Human samples. Cited in 7 publications.
View Alternative Names
VPS15, PIK3R4, Phosphoinositide 3-kinase regulatory subunit 4, PI3-kinase regulatory subunit 4, PI3-kinase p150 subunit, Phosphoinositide 3-kinase adaptor protein
- WB
Unknown
Western blot - Anti-VPS15 antibody [EPR5302(2)] (AB128903)
This antibody detects high background.
Blocking/Diluting buffer : 5% NFDM/TBST
All lanes:
Western blot - Anti-VPS15 antibody [EPR5302(2)] (ab128903) at 1/1000 dilution
All lanes:
Raji (Human Burkitt's lymphoma B lymphocyte) whole cell lysates at 15 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 153 kDa
Observed band size: 150 kDa
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- WB
Unknown
Western blot - Anti-VPS15 antibody [EPR5302(2)] (AB128903)
Blocking/Diluting buffer : 5% NFDM/TBST
This antibody detects high background.
All lanes:
Western blot - Anti-VPS15 antibody [EPR5302(2)] (ab128903) at 1/500 dilution
Lane 1:
Mouse E14.5 brain lysates at 20 µg
Lane 2:
Rat E14 brain lysates at 20 µg
Lane 3:
Rat P0 brain lysates at 20 µg
Lane 4:
C6 (Rat glial tumor glial cell) whole cell lysates at 20 µg
Lane 5:
Neuro-2a (Mouse neuroblastoma neuroblast) whole cell lysates at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 153 kDa
Observed band size: 150 kDa
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- OI-RD Scanning
Unknown
OI-RD Scanning - Anti-VPS15 antibody [EPR5302(2)] (AB128903)
We have systematically measured KD (the equilibrium dissociation constant between the antibody and its antigen), of more than 840 recombinant antibodies to assess not only their individual KD values but also to see the average affinity of antibody. Based on the comparison with published literature values for mouse monoclonal antibodies, Recombinant antibodies appear to be on average 1-2 order of magnitude higher affinity.
- WB
CiteAb
Western blot - Anti-VPS15 antibody [EPR5302(2)] (AB128903)
VPS15 western blot using anti-VPS15 antibody [EPR5302(2)] ab128903. Publication image and figure legend from Wang, M., Tang, C., et al., 2021, Mol Psychiatry, PubMed 30531936.
ab128903 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 ab128903 please see the product overview.
WDR81 suppresses PI3K-III activity in aNPCs. a Analysis of PI3K activity in Wdr81f/f aNPCs infected with lenti-dCreGFP or lenti-CreGFP (dCre vs. Cre, t test, p = 0.049; dCre, n = 3 independent experiments, Cre, n = 3 independent experiments). b 2xFYVE-mCherry-positive endosomes in Wdr81f/f aNPCs infected with lenti-CreGFP or lenti-dCreGFP. Scale bars, 5 μm. c Analysis of the size of 2xFYVE-mCherry endosomes in Wdr81f/f aNPCs infected with lenti-dCreGFP or lenti-CreGFP (dCre vs. Cre, t test, p < 0.0001; n = 20 cells from three independent experiments). d PtdIns3P ELISA analysis of Wdr81f/f aNPCs infected with lenti-dCreGFP or lenti-dCreGFP (dCre vs. Cre, t test, p = 0.036; dCre, n = 3 independent experiments, Cre, n = 3 independent experiments). e–g Co-IP of FLAG-WDR81 with HA-Beclin1, V5-VPS15, and GFP-VPS34. h and i Co-IP of VPS15 with VPS34 in WT and WDR81 KO cells (h) and quantification of the co-IP efficacy normalized to input (i, IP : VPS34, WT vs. KO, t test, p = 0.013; IP : VPS15, WT vs. KO, t test, p = 0.044; WT, n = 3 independent experiments, KO, n = 3 independent experiments). j and k Co-IP of Beclin1 with VPS34 in WT and WDR81 KO cells (j) and quantification of the co-IP efficacy normalized to input (k, IP : VPS34, WT vs. KO, t test, p = 0.514; IP : Beclin1, WT vs. KO, t test, p = 0.961, WT, n = 3 independent experiments, KO, n = 3 independent experiments). l Experimental scheme for assessing the proliferation and differentiation of aNPCs in the DG of adult hippocampus after TAM injection and 3-MA treatment. m Sample images of the DG stained with BrdU, Sox2, and GFAP at 2 h after BrdU injection. Scale bars, 20 μm. n Quantification of BrdU+GFAP-Sox2+ cells in the DG of Wdr81 cKO mice and WT mice treated with or without 3-MA at 2 h after BrdU injection (WT vs. WT + 3-MA, t test, p = 0.043; and cKO vs. cKO + 3-MA, t test, p = 0.014; WT, n = 5 mice, WT + 3-MA, n = 4 mice, cKO, n = 5 mice, cKO + 3-MA, n = 5 mice). o Sample images of the DG stained with BrdU and NeuN at 4 weeks after BrdU injection. Scale bars, 20 μm. p Quantification of BrdU+NeuN+ neurons in the DG of Wdr81 cKO mice and WT mice treated with 3-MA at 4 weeks after BrdU labeling (WT vs. WT + 3-MA, t test, p = 0.025; and cKO vs. cKO + 3-MA, t test, p = 0.012; WT, n = 5 mice, WT + 3-MA, n = 4 mice, cKO, n = 5 mice, cKO + 3-MA, n = 5 mice). Data are presented as mean ± SEM; *p < 0.05, ***p < 0.001
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Related conjugates and formulations (1)
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Anti-VPS15 antibody [EPR5302(2)] - BSA and Azide free
Reactivity data
Product details
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.
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Target data
Publications (7)
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The EMBO journal 43:931-955 PubMed38360997
2024
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Nature communications 13:4146 PubMed35842429
2022
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Neural regeneration research 17:1609-1616 PubMed34916448
2021
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eLife 8: PubMed31294692
2019
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Molecular psychiatry 24:1369-1382 PubMed30899091
2019
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Molecular psychiatry : PubMed30531936
2018
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Nature neuroscience 21:207-217 PubMed29311744
2018
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Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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