Anti-BTG2/PC3 antibody
3
(1 Review)
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(14 Publications)
Rabbit Polyclonal BTG2/PC3 antibody. Suitable for WB, IHC-P and reacts with Human samples. Cited in 14 publications. Immunogen corresponding to Synthetic Peptide within Human BTG2.
View Alternative Names
PC3, BTG2, Protein BTG2, BTG family member 2, NGF-inducible anti-proliferative protein PC3
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-BTG2/PC3 antibody (AB85051)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human fetal colon tissue labelling BTG2/PC3 with ab85051 at a dilution of 1/100.
- WB
Unknown
Western blot - Anti-BTG2/PC3 antibody (AB85051)
All lanes:
Western blot - Anti-BTG2/PC3 antibody (ab85051) at 1/250 dilution
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HepG2 cell lysates
Predicted band size: 17 kDa
Observed band size: 18 kDa
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- WB
CiteAb
Western blot - Anti-BTG2/PC3 antibody (AB85051)
BTG2/PC3 western blot using anti-BTG2/PC3 antibody ab85051. Publication image and figure legend from Shang, D., Xie, C., et al., 2020, J Cell Mol Med, PubMed 31724333.
ab85051 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 ab85051 please see the product overview.
PANC-1-exo carries miR-27a into HMVEC. A, The structure of exosomes identified by TEM (20 000×). B and C, The level of exosome surface marker CD63 in with or without exosomes measured by flow cytometry. D, The expression of miR-27a in exosomes extracted from H6c7 and PANC-1 cells. E, The uptake of exosomes by HMEC-1 cells following the delivery of Exo-depl, PANC-1-exo or miR-27a mimic (400×). F, VEGF level in the co-culture medium of PANC-1-exo and HMEC-1 cells following the delivery of Exo-depl, PANC-1-exo or miR-27a mimic, as measured by ELISA. G, The expression of miR-27a and BTG2 in HMEC-1 cells following the delivery of Exo-depl, PANC-1-exo or miR-27a mimic. H and I, Protein level of BTG2 in HMEC-1 cells following the delivery of Exo-depl, PANC-1-exo or miR-27a mimic. *p < .05 vs the treatment without exosomes or with exosomes secreted by H6c7. The above data are measurement data and described as mean ± standard deviation. Comparisons among multiple groups are analysed by one-way analysis of variance. n = 12. The experiment was repeated 3 times independently. miR-27a, microRNA-27a; exo, exosomes; BTG2, B-cell translocation gene 2; PC, pancreatic cancer; HMVEC, human microvascular endothelial cell; VEGF, vascular endothelial growth factor; TEM, transmission electron microscope; ELISA, enzyme-linked immunoassay
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Reactivity data
Properties and storage information
Form
Reconstitution
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The BTG2 protein plays an important role in controlling cell cycle progression and apoptosis. It negatively regulates the transition from the G1 phase to the S phase of the cell cycle by interacting with cyclin D1 and E2F-1 transcription factors which are critical for DNA synthesis initiation. Additionally BTG2 does not operate as part of a larger protein complex but can impact the activity and stability of other transcription factors and proteins. Its ability to modulate different cellular processes highlights its importance in maintaining normal cell function and preventing uncontrolled proliferation.
Pathways
BTG2 is integrated into the tumor suppressor network and influences gene transcription and mRNA degradation pathways. It is connected to the p53 pathway where it functions downstream of p53 a protein that responds to stress signals and maintains genomic stability. BTG2's relationship with the p53 pathway also aligns it with proteins such as MDM2 which helps regulate p53 turnover. This pathway connection showcases BTG2's role in mediating DNA damage responses and maintaining cellular integrity.
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Publications (14)
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Frontiers in pharmacology 16:1559546 PubMed40115255
2025
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Cell reports. Medicine 5:101777 PubMed39413736
2024
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Discover oncology 15:401 PubMed39225900
2024
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Molecular cancer 22:135 PubMed37580748
2023
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Acta biochimica et biophysica Sinica 54:1775-1788 PubMed36789695
2023
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Bioengineered 12:9507-9519 PubMed34699325
2021
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Science progress 104:368504211002043 PubMed33844600
2021
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Journal of cellular and molecular medicine 25:4671-4683 PubMed33811437
2021
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Frontiers in oncology 10:547942 PubMed33425718
2020
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The journal of gene medicine 23:e3280 PubMed33025678
2020
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Product promise
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