Anti-Cyclin A2 antibody [EPR17351]
- RabMAb
- Recombinant
- 20ul selling size
- What is this?
5
(3 Reviews)
|
(135 Publications)
Anti-Cyclin A2 antibody [EPR17351] (ab181591) is a rabbit monoclonal antibody detecting Cyclin A2 in Western Blot, IHC-P, ICC/IF. Suitable for Human, Mouse, Rat.
- Biophysical QC for unrivalled batch-batch consistency
- Over 90 publications
View Alternative Names
CCN1, CCNA, CCNA2, Cyclin-A2, Cyclin-A, Cyclin A
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cyclin A2 antibody [EPR17351] (AB181591)
Immunohistochemical analysis of paraffin-embedded Human cervix carcinoma tissue labeling Cyclin A2 with ab181591 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Nuclear and weak cytoplasmic staining on some tumor cells in Human cervix carcinoma tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cyclin A2 antibody [EPR17351] (AB181591)
Immunohistochemical analysis of paraffin-embedded Human tonsil tissue labeling Cyclin A2 with ab181591 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Nuclear and weak cytoplasmic staining on germinal center cells of Human tonsil tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Cyclin A2 antibody [EPR17351] (AB181591)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa (Human epithelial cell line from cervix adenocarcinoma) cells labeling Cyclin A2 with ab181591 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Confocal image showing nuclear and weakly cytoplasmic staining on HeLa cells. The nuclear counter stain is DAPI (blue).
Tubulin is detected with Anti-alpha Tubulin antibody [EPR17351]- Loading Control (ab7291) at 1/1000 dilution, followed by Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed (ab150120) at 1/1000 dilution (red).
The negative controls are as follows :
-ve control 1 : ab181591 at 1/500 dilution, followed by Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed (ab150120) at 1/500 dilution.
-ve control 2 : Anti-alpha Tubulin antibody [EPR17351]- Loading Control (ab7291) at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cyclin A2 antibody [EPR17351] (AB181591)
Immunohistochemical analysis of paraffin-embedded mouse endometrium tissue labeling Cyclin A2 with ab181591 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Nuclear and weak cytoplasmic staining on a proportion of epithelial cells in mouse endometrial tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cyclin A2 antibody [EPR17351] (AB181591)
Immunohistochemical analysis of paraffin-embedded rat colon tissue labeling Cyclin A2 with ab181591 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Nuclear and weak cytoplasmic staining on a proportion of epithelial cells in rat colon tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- WB
Supplier Data
Western blot - Anti-Cyclin A2 antibody [EPR17351] (AB181591)
Blocking/Dilution buffer : 5% NFDM/TBST.
The smaller band is due to a tissue-specific splice variant, PMID 22745723.
All lanes:
Western blot - Anti-Cyclin A2 antibody [EPR17351] (ab181591) at 1/2000 dilution
All lanes:
Human fetal kidney lysate at 10 µg
Secondary
All lanes:
Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 22 kDa,49 kDa,84 kDa
Observed band size: 110 kDa,18 kDa,22 kDa,50 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-Cyclin A2 antibody [EPR17351] (AB181591)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Cyclin A2 antibody [EPR17351] (ab181591) at 1/20000 dilution
All lanes:
Human tonsil lysate at 10 µg
Secondary
All lanes:
Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 49 kDa
Observed band size: 50 kDa
false
Exposure time: 1min
- WB
Supplier Data
Western blot - Anti-Cyclin A2 antibody [EPR17351] (AB181591)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Cyclin A2 antibody [EPR17351] (ab181591) at 1/20000 dilution
All lanes:
Jurkat (Human T cell leukemia cell line from peripheral blood) whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 49 kDa
Observed band size: 50 kDa
false
Exposure time: 10s
- WB
Supplier Data
Western blot - Anti-Cyclin A2 antibody [EPR17351] (AB181591)
Blocking/Dilution buffer : 5% NFDM/TBST.
Cyclin A2 is down regulated at the G2/M phase.
All lanes:
Western blot - Anti-Cyclin A2 antibody [EPR17351] (ab181591) at 1/20000 dilution
Lane 1:
HeLa (Human epithelial cell line from cervix adenocarcinoma) lysate; Untreated, asynchronous cells (<a href='/en-us/products/unavailable/hela-cell-cycle-lysates-thymidine-treated-nocodazole-treated-untreated-asynchronous-control-ab136811'>ab136811</a>) at 1 µg
Lane 2:
HeLa (Human epithelial cell line from cervix adenocarcinoma) lysate; G1/S arrested cells (thymidine treatment) (<a href='/en-us/products/unavailable/hela-cell-cycle-lysates-thymidine-treated-nocodazole-treated-untreated-asynchronous-control-ab136811'>ab136811</a>) at 1 µg
Lane 3:
HeLa (Human epithelial cell line from cervix adenocarcinoma) lysate; G2/M arrested cells (sequential thymidine and nocodazole treatments) (<a href='/en-us/products/unavailable/hela-cell-cycle-lysates-thymidine-treated-nocodazole-treated-untreated-asynchronous-control-ab136811'>ab136811</a>) at 1 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated or Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 49 kDa
Observed band size: 50 kDa
false
Exposure time: 30s
- WB
Supplier Data
Western blot - Anti-Cyclin A2 antibody [EPR17351] (AB181591)
Blocking/Dilution buffer : 5% NFDM/TBST.
The smaller band is due to a tissue-specific splice variant, PMID 22745723.
All lanes:
Western blot - Anti-Cyclin A2 antibody [EPR17351] (ab181591) at 1/2000 dilution
All lanes:
Rat spleen lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 49 kDa
Observed band size: 50 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-Cyclin A2 antibody [EPR17351] (AB181591)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Cyclin A2 antibody [EPR17351] (ab181591) at 1/2000 dilution
Lane 1:
C6 (Rat glial tumor cell line) whole cell lysate at 10 µg
Lane 2:
RAW 264.7 (Mouse macrophage cell line transformed with Abelson murine leukemia virus) whole cell lysate at 10 µg
Lane 3:
PC-12 (Rat adrenal gland pheochromocytoma cell line) whole cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L),Peroxidase conjugated at 1/1000 dilution
Predicted band size: 49 kDa
Observed band size: 50 kDa
false
Exposure time: 3s
Related conjugates and formulations (4)
-
Anti-Cyclin A2 antibody [EPR17351] - BSA and Azide free
-
565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-Cyclin A2 antibody [EPR17351]
-
617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-Cyclin A2 antibody [EPR17351]
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-Cyclin A2 antibody [EPR17351]
Reactivity data
Product details
What is this antibody validated in?
Anti-Cyclin A2 antibody [EPR17351] (ab181591) is a rabbit recombinant monoclonal antibody and is validated for use in Western Blot (WB), Immunohistochemistry (IHC-P), Immunocytochemistry/immunofluorescence (ICC/IF) in Human, Mouse, Rat samples.
What is the molecular weight of Cyclin A2?
Anti-Cyclin A2 [EPR17351] (ab181591) specifically detects a band for Cyclin A2 (UniProt: P51943) at a molecular weight of 47kDa.
Trusted by the scientific community
Anti-Cyclin A2 [EPR17351] (ab181591) was first used in a scientific publication in 2015 and has been cited over 90 times in peer-reviewed journals.
Trial sizes available!
Test your antibody or perform pre-screening before committing to a larger quantity. Sold in 10µl. Discover our selection of trial-size antibodies.
Other related products
We have a range of other formats of antibody clone [EPR17351] also available for your convenience: ab181591, Alexa Fluor® 647 - ab216303, Alexa Fluor® 594 - ab217226, Alexa Fluor® 555 - ab217731, Carrier free - ab231164
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
Form
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
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (135)
Recent publications for all applications. Explore the full list and refine your search
The Tohoku journal of experimental medicine : PubMed41062300
2025
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Discover oncology 16:1763 PubMed41021168
2025
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Cancer management and research 17:1657-1666 PubMed40837329
2025
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World journal of gastrointestinal oncology 17:106781 PubMed40837761
2025
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Leukemia 39:2789-2800 PubMed40813622
2025
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International journal of biological sciences 21:3934-3948 PubMed40612684
2025
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Nature 642:785-795 PubMed40399682
2025
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Frontiers in cell and developmental biology 13:1561815 PubMed40376613
2025
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Nature 641:1309-1318 PubMed40307557
2025
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Cell & bioscience 15:48 PubMed40247362
2025
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com