重组Anti-RPA32/RPA2 (phospho T21)抗体[EPR2846(2)]
Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)]
- RabMAb
- Recombinant
- 了解详情
4
(1 Review)
|
(32 Publications)
Rabbit Recombinant Monoclonal RPA32/RPA2 phospho T21 antibody. Suitable for ELISA, Dot, WB and reacts with Recombinant fragment - Human, Mouse, Rat, Human samples. Cited in 32 publications.
查看别名
REPA2, RPA32, RPA34, RPA2, Replication protein A 32 kDa subunit, RP-A p32, Replication factor A protein 2, Replication protein A 34 kDa subunit, RF-A protein 2, RP-A p34
- ELISA
Supplier Data
ELISA - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (AB109394)
Direct ELISA antigen dose-response curve using purified ab109394.
Primary antibody : ab109394 (0-1000nweg/ml).
Antigens : P1 : Human RPA32/RPA2 (phospho T21) at 10ng/ml and 1ng/ml; NP : non-phospho at 10ng/ml and 1 ng/ml.
Secondary antibody : Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L) at 1/2500 dilution.
- WB
Lab
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (AB109394)
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (ab109394) at 1/50000 dilution
Lane 1:
HeLa whole cell lysate - untreated at 10 µg
Lane 2:
HeLa whole cell lysate - treated with Calyculin A at 10 µg
Lane 3:
HeLa whole cell lysate - treated with Calyculin A and Alkaline Phosphatase at 10 µg
Secondary
All lanes:
Peroxidase-conjugated goat anti-rabbit IgG (H+L) at 1/1000 dilution
Predicted band size: 29 kDa
Observed band size: 32 kDa
false
Exposure time: 30s
- WB
Supplier Data
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (AB109394)
Blocking/Diluting buffer and concentration : 5% NFDM/TBST
All lanes:
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (ab109394) at 1/5000 dilution
Lane 1:
MDA-MB-231 (Human breast adenocarcinoma epithelial cell) whole cell lysates at 15 µg
Lane 2:
MDA-MB-231 (Human breast adenocarcinoma epithelial cell) whole cell lysates. Then the membrane was incubated with phosphatase. at 15 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: 29 kDa
Observed band size: 32 kDa,36 kDa
false
Exposure time: 30s
- WB
Unknown
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (AB109394)
All lanes:
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (ab109394) at 1/50000 dilution
Lane 1:
HeLa cell lysates, untreated at 10 µg
Lane 2:
HeLa cell lysates, treated with Camptothecin at 10 µg
Predicted band size: 29 kDa
Observed band size: 32 kDa
false
- Dot
Supplier Data
Dot Blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (AB109394)
Dot blot analysis of human c-Myb RPA32/RPA2 (pT21) phospho peptide (Lane 1) and RPA32/RPA2 non-phospho peptide (Lane 2) labeling RPA32/RPA2 (phospho T21) with purified ab109394 at a dilution of 1/5000. ab97051 (Peroxidase conjugated goat anti-rabbit IgG (H+L)) was used as the secondary antibody at a dilution of 1/2500.
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure time : 3 minutes.
- Dot
Lab
Dot Blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (AB109394)
Dot blot analysis of RPA32/RPA2 (pT21) phospho peptide (lane 1) and RPA32/RPA2 non-phospho peptide (lane 2) labelling RPA32/RPA2 (phospho T21) with ab109394 at a dilution of 1/1000. A peroxidase-conjugated goat anti-rabbit IgG (H+L) was used as the secondary antibody (1/2500).
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure time : 3 minutes.
- WB
Supplier Data
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (AB109394)
Blocking/Diluting buffer and concentration : 5% NFDM/TBST.
Exposure time : 110 seconds.
All lanes:
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (ab109394) at 1/2000 dilution
Lane 1:
C6 (Rat glial tumor glial cell) whole cell lysates at 15 µg
Lane 2:
C6 (Rat glial tumor glial cell) treated with 100nM calyculin A for 60 minutes whole cell lysates at 15 µg
Lane 3:
C6 (Rat glial tumor glial cell) treated with 100nM calyculin A for 60 minutes whole cell lysates. Then the membrane was incubated with phosphatase at 15 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: 29 kDa
Observed band size: 32 kDa,36 kDa
false
- WB
Supplier Data
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (AB109394)
Blocking/Diluting buffer and concentration : 5% NFDM/TBST.
Exposure time : 180 seconds.
All lanes:
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (ab109394) at 1/2000 dilution
Lane 1:
NIH/3T3 (Mouse embryonic fibroblast) whole cell lysates at 15 µg
Lane 2:
NIH/3T3 (Mouse embryonic fibroblast) treated with 100ng/ml calyculin A for 30 minutes whole cell lysates at 15 µg
Lane 3:
NIH/3T3 (Mouse embryonic fibroblast) treated with 100ng/ml calyculin A for 60 3minutes whole cell lysates.Then the membrane was incubated with phosphatase at 15 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: 29 kDa
Observed band size: 32 kDa,36 kDa
false
- WB
CiteAb
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (AB109394)
Western Blotting using Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)], ab109394. Publication image from Kim, W. et al., 2019, Nat Commun, 31757956. Legend direct from paper.
ZFP161 is enriched at replication forks. a Cells were depleted of RPA32 using shRNA. The co-localization of phospho-RPA32 (S4/S8) and ZFP161 were determined by immunofluorescence. b RPA32 deficient HCT116 cells were incubated with EdU and HU. Replication fork proteins were isolated by iPOND and immunoblotted with indicated antibodies. c Cells were depleted of ZFP161 using sgRNA. The co-localization of RPA32 and γH2AX were determined by immunofluorescence. d ZFP161 deficient HCT116 cells were incubated with EdU and HU. Replication fork proteins were isolated by iPOND and immunoblotted with indicated antibodies. e Purified GST-ZFP161 protein and RPA complex were incubated with biotin labeled single fork DNA. The proteins retained on DNA were determined by immunoblotting. Scale bars, 10 µm. Source data are provided as a Source Data file.
false
- WB
CiteAb
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (AB109394)
Western Blotting using Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)], ab109394. Publication image from Kim, W. et al., 2019, Nat Commun, 31757956. Legend direct from paper.
ZFP161 is important for ATR activation. a The co-localization of phospho-RPA32 (S4/S8) and ZFP161 was determined by immunofluorescence in control or ZFP161-deficent cells. b After 10 mM HU treatment for 2 h, phosphorylation of DNA damage related proteins was determined by immunoblotting in ZFP161-knockout HCT116 cells. Scale bars, 10 µm. Source data are provided as a Source Data file.
false
- WB
CiteAb
Western blot - Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] (AB109394)
Western Blotting using Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)], ab109394. Publication image from Kim, W. et al., 2019, Nat Commun, 31757956. Legend direct from paper.
ZFP161 is enriched at replication forks. a Cells were depleted of RPA32 using shRNA. The co-localization of phospho-RPA32 (S4/S8) and ZFP161 were determined by immunofluorescence. b RPA32 deficient HCT116 cells were incubated with EdU and HU. Replication fork proteins were isolated by iPOND and immunoblotted with indicated antibodies. c Cells were depleted of ZFP161 using sgRNA. The co-localization of RPA32 and γH2AX were determined by immunofluorescence. d ZFP161 deficient HCT116 cells were incubated with EdU and HU. Replication fork proteins were isolated by iPOND and immunoblotted with indicated antibodies. e Purified GST-ZFP161 protein and RPA complex were incubated with biotin labeled single fork DNA. The proteins retained on DNA were determined by immunoblotting. Scale bars, 10 µm. Source data are provided as a Source Data file.
false
不同偶联物与剂型 (1)
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Anti-RPA32/RPA2 (phospho T21) antibody [EPR2846(2)] - 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.
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运输条件
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分装信息
储存信息
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- Visit the General protocols
- Visit the Troubleshooting
靶点信息
文献 (32)
Recent publications for all applications. Explore the full list and refine your search
The Journal of clinical investigation 135: PubMed40794452
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The Journal of biological chemistry 299:105385 PubMed37890780
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The Journal of cell biology 222: PubMed37036693
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Applied biochemistry and biotechnology 195:3477-3490 PubMed36607481
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Nature cell biology 23:1095-1104 PubMed34616022
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Translational oncology 14:101167 PubMed34280886
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Molecular cell 81:724-738.e9 PubMed33476576
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Proceedings of the National Academy of Sciences of the United States of America 118: PubMed33431668
2021
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