Anti-PCNA antibody [24/PCNA] - BSA and Azide free (ab280093)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Mouse monoclonal [24/PCNA] to PCNA - BSA and Azide free
- Suitable for: WB, ICC, IHC-P
- Reacts with: Mouse, Rat, Human
Overview
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Product name
Anti-PCNA antibody [24/PCNA] - BSA and Azide free
See all PCNA primary antibodies -
Description
Mouse monoclonal [24/PCNA] to PCNA - BSA and Azide free -
Host species
Mouse -
Tested applications
Suitable for: WB, ICC, IHC-Pmore details -
Species reactivity
Reacts with: Mouse, Rat, Human -
Immunogen
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- WB: HeLa, C6, RAW264.7, PC-12, NIH/3T3, Jurkat and A431 cell lysate. IHC-P: Human tonsil and colon tissue. Mouse and rat spleen tissue. ICC: HeLa, NIH/3T3 and C6 cells.
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General notes
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com.
ab280093 is the carrier-free version of ab280088. This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.
Our carrier-free formats are supplied in a buffer free of BSA, sodium azide and glycerol for higher conjugation efficiency.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with
ab280093 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.
Maxpar® is a trademark of Fluidigm Canada Inc.
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 production
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. Do Not Freeze. -
Storage buffer
Constituent: 100% PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
24/PCNA -
Isotype
IgG1
Images
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All lanes : Anti-PCNA antibody [24/PCNA] (ab280088) at 1/1000 dilution
Lane 1 : HeLa (human cervix adenocarcinoma epithelial cell ), whole cell lysate
Lane 2 : Jurkat (human T cell leukemia T lymphocyte), whole cell lysate
Lane 3 : A431 (human epidermoid carcinoma epithelial cell), whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
Predicted band size: 29 kDa
Exposure time: 26 secondsThis data was developed using ab280088 the same antibody clone in a different buffer formulation.
Blocking/Dilution buffer: 5% NFDM/TBST.
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This data was developed using ab280088 the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human tonsil tissue labeling PCNA with ab280088 at 1/5000 (0.215 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Nuclear staining on human tonsil.
The section was incubated with ab280088 for 30 minutes at room temperature and followed by rabbit specific IgG antibody ab125913 for 8 minutes. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control: Secondary antibody is ready to use LeicaDS9800 (Bond® Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 minutes.
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This data was developed using ab280088 the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol-fixed, 0.1% Triton X-100 permeabilized HeLa cells labelling PCNA with ab280088 at 1/20 (53.7 µg/ml) dilution, followed by ab150113 Goat Anti-mouse IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (Green). Confocal image showing nuclear staining in HeLa cell line.
ab179513 anti-beta Tubulin rabbit monoclonal antibody was used to counterstain tubulin at 1/200 dilution followed by ab150080 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) at a 1/500 dilution (Red). The nuclear counterstain was DAPI (Blue).
Negative control 1: ab280088 at a 1/20 dilution followed by ab150080 at a 1/500 dilution.
Negative control 2: ab179513 at a 1/200 dilution followed by ab150113 at a 1/1000 dilution.
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All lanes : Anti-PCNA antibody [24/PCNA] (ab280088) at 1/1000 dilution
Lane 1 : C6 (rat glial tumor glial cell), whole cell lysate
Lane 2 : RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage), whole cell lysate
Lane 3 : PC-12 (rat adrenal gland pheochromocytoma), whole cell lysate
Lane 4 : NIH/3T3 (mouse embryonic fibroblast), whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
Predicted band size: 29 kDa
Exposure time: 6 secondsThis data was developed using ab280088 the same antibody clone in a different buffer formulation.
Blocking/Dilution buffer: 5% NFDM/TBST.
-
This data was developed using ab280088 the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human colon tissue labeling PCNA with ab280088 at 1/5000 (0.215 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Nuclear staining on human colon.
The section was incubated with ab280088 for 30 minutes at room temperature and followed by rabbit specific IgG antibody ab125913 for 8 minutes. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control: Secondary antibody is ready to use LeicaDS9800 (Bond® Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 minutes.
-
This data was developed using ab280088 the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse spleen tissue labeling PCNA with ab280088 at 1/5000 (0.215 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Nuclear staining on mouse spleen.
The section was incubated with ab280088 for 30 minutes at room temperature and followed by rabbit specific IgG antibody ab125913 for 8 minutes. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control: Secondary antibody is ready to use LeicaDS9800 (Bond® Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 minutes.
-
This data was developed using ab280088 the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat spleen tissue labeling PCNA with ab280088 at 1/5000 (0.215 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Nuclear staining on rat spleen.
The section was incubated with ab280088 for 30 minutes at room temperature and followed by rabbit specific IgG antibody ab125913 for 8 minutes. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control: Secondary antibody is ready to use LeicaDS9800 (Bond® Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 minutes.
-
This data was developed using ab280088 the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol-fixed, 0.1% Triton X-100 permeabilized C6 cells labelling PCNA with ab280088 at 1/20 (53.7 µg/ml) dilution, followed by ab150113 Goat Anti-mouse IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (Green).
Confocal image showing nuclear and weak cytoplasmic staining in C6 cell line.
ab179513 anti-beta Tubulin rabbit monoclonal antibody was used to counterstain tubulin at 1/200 dilution followed by ab150080 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) at a 1/500 dilution (Red). The nuclear counterstain was DAPI (Blue).
Negative control 1: ab280088 at a 1/20 dilution followed by ab150080 at a 1/500 dilution.
Negative control 2: ab179513 at a 1/200 dilution followed by ab150113 at a 1/1000 dilution.
-
This data was developed using ab280088 the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol-fixed, 0.1% Triton X-100 permeabilized NIH/3T3 cells labelling PCNA with ab280088 at 1/20 (53.7 µg/ml) dilution, followed by ab150113 Goat Anti-mouse IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (Green).
Confocal image showing nuclear staining in NIH/3T3 cell line.
ab179513 anti-beta Tubulin rabbit monoclonal antibody was used to counterstain tubulin at 1/200 dilution followed by ab150080 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) at a 1/500 dilution (Red). The nuclear counterstain was DAPI (Blue).
Negative control 1: ab280088 at a 1/20 dilution followed by ab150080 at a 1/500 dilution.
Negative control 2: ab179513 at a 1/200 dilution followed by ab150113 at a 1/1000 dilution.
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