Anti-RPA32/RPA2 antibody [EPR22950-81]
- BOND RX™ Validated
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal RPA32/RPA2 antibody. Suitable for IP, WB, ICC/IF, Flow Cyt (Intra), IHC-P and reacts with Human samples. Cited in 1 publication.
View Alternative Names
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
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-RPA32/RPA2 antibody [EPR22950-81] (AB240637)
Intracellular flow cytometric analysis of 4% paraformaldehyde fixed. 90% methanol permeabilized HeLa (human cervix adenocarcinoma epithelial cell) cells labeling RPA32/RPA2 with ab240637 at 1/600 dilution (Red) compared with a Rabbit monoclonal IgG (ab172730) isotype control (black)and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-RPA32/RPA2 antibody [EPR22950-81] (AB240637)
Immunohistochemical analysis of paraffin-embedded human glioma tissue labeling RPA32/RPA2 with ab240637 at 1/5000 dilution (0.103 ug/ml) followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Nuclear staining on human glioma (PMID : 20154705) is observed. The section was incubated with ab240637 for 10 mins at RT. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 6.0, epitope retrieval solution 1) for 20 mins.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-RPA32/RPA2 antibody [EPR22950-81] (AB240637)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa (human cervix adenocarcinoma epithelial cell) cells labeling RPA32/RPA2 with ab240637 at 1/100 dilution, followed by anti-RPA32/RPA2 ab150077 AlexaFluor®488 Goat anti-Rabbit secondary antibody at 1/1000 dilution (Green). Confocal image showing nuclear staining in HeLa cell line is observed. ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is AlexaFluor®488 Goat anti-Rabbit secondary (ab150077) at 1/1000 dilution.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-RPA32/RPA2 antibody [EPR22950-81] (AB240637)
Immunohistochemical analysis of paraffin-embedded human colon tissue labeling RPA32/RPA2 with ab240637 at 1/5000 dilution (0.103 ug/ml) followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Nuclear staining on human colon (PMID : 20154705) is observed. The section was incubated with ab240637 for 10 mins at RT. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 6.0, epitope retrieval solution 1) for 20 mins.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
- IP
Unknown
Immunoprecipitation - Anti-RPA32/RPA2 antibody [EPR22950-81] (AB240637)
RPA32/RPA2 was immunoprecipitated from 0.35 mg HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate with ab240637 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab240637 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate 10μg.
Lane 2 : ab240637 IP in HeLa whole cell lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab240637 in HeLa whole cell lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 8 seconds.
All lanes:
Immunoprecipitation - Anti-RPA32/RPA2 antibody [EPR22950-81] (ab240637)
Predicted band size: 29 kDa
Observed band size: 32 kDa
false
- WB
Lab
Western blot - Anti-RPA32/RPA2 antibody [EPR22950-81] (AB240637)
Exposure time : 5.5 seconds.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-RPA32/RPA2 antibody [EPR22950-81] (ab240637) at 1/1000 dilution
All lanes:
Human brain tissue lysate 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 1/100000 dilution
Predicted band size: 29 kDa
Observed band size: 32 kDa
false
- WB
Lab
Western blot - Anti-RPA32/RPA2 antibody [EPR22950-81] (AB240637)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The molecular weight of RPA32/RPA2 is upshifted in response to camptothecin treatment (PMID : 17928296).
To minimize protein degradation, cells were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-RPA32/RPA2 (phospho S33) antibody [EPR29612-551] (<a href='/en-us/products/primary-antibodies/rpa32-rpa2-phospho-s33-antibody-epr29612-551-ab325750'>ab325750</a>) at 1/1000 dilution
Lane 1:
Untreated 293T (human embryonic kidney epithelial cell) fresh whole cell lysate (untreated membrane) at 50 µg
Lane 2:
293T treated with 1 μM camptothecin for 3 h fresh whole cell lysate (untreated membrane) at 50 µg
Lane 3:
Untreated 293T (human embryonic kidney epithelial cell) fresh whole cell lysate (alkaline phosphatase treated membrane) at 50 µg
Lane 4:
293T treated with 1 μM camptothecin for 3 h fresh whole cell lysate (alkaline phosphatase treated membrane) at 50 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
Observed band size: 32 kDa,36 kDa,30 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-RPA32/RPA2 antibody [EPR22950-81] (AB240637)
Exposure time : 5.5 seconds.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-RPA32/RPA2 antibody [EPR22950-81] (ab240637) at 1/1000 dilution
Lane 1:
HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate at 20 µg
Lane 2:
HUVEC (human umbilical vein endothelial cell), whole cell lysate at 20 µg
Lane 3:
U-2 OS (human bone osteosarcoma epithelial cell), whole cell lysate 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 1/100000 dilution
Predicted band size: 29 kDa
Observed band size: 32 kDa
false
- WB
Supplier Data
Western blot - Anti-RPA32/RPA2 antibody [EPR22950-81] (AB240637)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The molecular weight of RPA32/RPA2 is upshifted in response to Etoposide treatment (PMID : 21731742).
To minimize protein degradation, cells were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
In Western blot, Anti-RPA32/RPA2 antibody (ab240637) staining at 1/1000 dilution.
All lanes:
Western blot - Anti-RPA32/RPA2 (phospho S4) antibody [EPR29611-59] (<a href='/en-us/products/primary-antibodies/rpa32-rpa2-phospho-s4-antibody-epr29611-59-ab325317'>ab325317</a>) at 1/1000 dilution
Lane 1:
Untreated HeLa (human cervical adenocarcinoma epithelial cell) fresh whole cell lysate (untreated membrane) at 50 µg
Lane 2:
HeLa treated with 100µM Etoposide for 4h fresh whole cell lysate (untreated membrane) at 50 µg
Lane 3:
Untreated HeLa fresh whole cell lysate (alkaline phosphatase treated membrane) at 50 µg
Lane 4:
HeLa treated with 100µM Etoposide for 4h fresh whole cell lysate (alkaline phosphatase treated membrane) at 50 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
Observed band size: 32 kDa,30 kDa,36 kDa
false
Exposure time: 26s
- WB
Supplier Data
Western blot - Anti-RPA32/RPA2 antibody [EPR22950-81] (AB240637)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The molecular weight of RPA32/RPA2 is upshifted in response to camptothecin treatment (PMID : 21731742).
To minimize protein degradation, cells were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
In Western blot, Anti-RPA32/RPA2 antibody (ab240637) staining at 1/1000 dilution.
All lanes:
Western blot - Anti-RPA32/RPA2 (phospho S4) antibody [EPR29611-59] (<a href='/en-us/products/primary-antibodies/rpa32-rpa2-phospho-s4-antibody-epr29611-59-ab325317'>ab325317</a>) at 1/1000 dilution
Lane 1:
Untreated 293T (human embryonic kidney epithelial cell) fresh whole cell lysate (untreated membrane) at 50 µg
Lane 2:
293T treated with 1µM camptothecin for 3h fresh whole cell lysate (untreated membrane) at 50 µg
Lane 3:
Untreated 293T (human embryonic kidney epithelial cell) fresh whole cell lysate (alkaline phosphatase treated membrane) at 50 µg
Lane 4:
293T treated with 1µM camptothecin for 3h fresh whole cell lysate (alkaline phosphatase treated membrane) at 50 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
Observed band size: 32 kDa,30 kDa,36 kDa
false
Exposure time: 15s
- WB
Lab
Western blot - Anti-RPA32/RPA2 antibody [EPR22950-81] (AB240637)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The molecular weight of RPA32/RPA2 is upshifted in response to Etoposide treatment (PMID : 17928296).
To minimize protein degradation, cells were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-RPA32/RPA2 (phospho S33) antibody [EPR29612-551] (<a href='/en-us/products/primary-antibodies/rpa32-rpa2-phospho-s33-antibody-epr29612-551-ab325750'>ab325750</a>) at 1/1000 dilution
Lane 1:
Untreated HeLa (human cervical adenocarcinoma epithelial cell) fresh whole cell lysate at 50 µg
Lane 2:
HeLa treated with 100 μM Etoposide for 16 hours fresh whole cell lysate at 50 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
Observed band size: 32 kDa,36 kDa,30 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-RPA32/RPA2 antibody [EPR22950-81] (AB240637)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The molecular weight of RPA32/RPA2 is upshifted in response to camptothecin treatment (PMID : 21731742).
To minimize protein degradation, cells were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
In Western blot, Anti-RPA32/RPA2 antibody (ab240637) staining at 1/1000 dilution.
All lanes:
Western blot - Anti-RPA32/RPA2 (phospho S4) antibody [EPR29611-59] (<a href='/en-us/products/primary-antibodies/rpa32-rpa2-phospho-s4-antibody-epr29611-59-ab325317'>ab325317</a>) at 1/1000 dilution
Lane 1:
Untreated NIH/3T3 (mouse embryonic fibroblast) fresh whole cell lysate (untreated membrane) at 50 µg
Lane 2:
NIH/3T3 treated with 1µM camptothecin for 3h fresh whole cell lysate (untreated membrane) at 50 µg
Lane 3:
Untreated NIH/3T3 fresh whole cell lysate (alkaline phosphatase treated membrane) at 50 µg
Lane 4:
NIH/3T3 treated with 1µM camptothecin for 3h fresh whole cell lysate (alkaline phosphatase treated membrane) at 50 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
Observed band size: 32 kDa,30 kDa,36 kDa
false
Exposure time: 26s
Related conjugates and formulations (1)
-
Anti-RPA32/RPA2 antibody [EPR22950-81] - 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.
Properties and storage information
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Storage buffer
Shipped at conditions
Appropriate short-term storage duration
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Appropriate long-term storage conditions
Aliquoting information
Storage information
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Nature communications 16:3312 PubMed40204713
2025
Applications
Unspecified application
Species
Unspecified reactive species
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