Anti-PCNA antibody [16D10] - BSA and Azide free (ab255842)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rat monoclonal [16D10] to PCNA - BSA and Azide free
- Suitable for: ICC, IP
- Reacts with: Mouse, Rat, Human
Overview
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Product name
Anti-PCNA antibody [16D10] - BSA and Azide free
See all PCNA primary antibodies -
Description
Rat monoclonal [16D10] to PCNA - BSA and Azide free -
Host species
Rat -
Tested applications
Suitable for: ICC, IPmore 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
- ICC: NIH/3T3, HeLa and C6 cells. IP: NIH/3T3 cell lysate.
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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.
ab255842 is the carrier-free version of ab252848. 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
ab255842 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
pH: 7.2
Constituent: PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
16D10 -
Isotype
IgG2b -
Research areas
Images
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Immunocytochemical analysis of 100% methanol-fixed NIH/3T3 (mouse embryonic fibroblast) cells labeling PCNA (green) using ab252848 at 7.08µg/ml followed by ab150157 Goat Anti-Rat IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (2µg/ml). ab179504 Anti-beta IV Tubulin antibody was used as a counterstain at 1/200 dilution (10µg/ml) followed by ab150080 AlexaFluor®594 Goat anti-Rabbit secondary at 1/1000 dilution (2µg/ml) (Red). Confocal image showing nuclear staining in NIH/3T3 cell line. The nuclear counterdstain was DAPI (Blue).
-ve control 1: ab252848 (1/50 dilution) followed by ab150080 (1/1000 dilution).
-ve control 2: ab179504 (1/200 dilution) followed by ab150157 (1/1000 dilution).
This image was produced by the same antibody in a different buffer formulation containing PBS, BSA and sodium azide (ab252848).
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PCNA was immunoprecipitated from 0.35 mg NIH/3T3 (mouse embryonic fibroblast), whole cell lysate using ab252848 at 1/30 dilution (2µg in 0.35µg lysates). Western blot was performed on the immunoprecipitate using ab252848 at 1/1000 dilution (0.35µg/ml) followed by anti-Rat IgG H&L (HRP) (ab205720) secondary at 1/5000 dilution.
Lane 1: NIH/3T3 whole cell lysate 10 µg.
Lane 2: ab252848 IP in NIH/3T3 whole cell lysate.
Lane 3: Rat monoclonal IgG instead of ab252848 in NIH/3T3 whole cell lysate.
Blocking/Diluting buffer and concentration: 5% NFDM/TBST.
Exposure time: 1 second.
This image was produced by the same antibody in a different buffer formulation containing PBS, BSA and sodium azide (ab252848).
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Immunocytochemical analysis of 100% methanol-fixed C6 (rat glial tumor glial cell) cells labeling PCNA (green) using ab252848 at 7.08µg/ml followed by ab150157 Goat Anti-Rat IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (2µg/ml). ab179504 Anti-beta IV Tubulin antibody was used as a counterstain at 1/200 dilution (10µg/ml) followed by ab150080 AlexaFluor®594 Goat anti-Rabbit secondary at 1/1000 dilution (2µg/ml) (Red). Confocal image showing nuclear staining in C6 cell line. The nuclear counterdstain was DAPI (Blue).
-ve control 1: ab252848 (1/50 dilution) followed by ab150080 (1/1000 dilution).
-ve control 2: ab179504 (1/200 dilution) followed by ab150157 (1/1000 dilution).
This image was produced by the same antibody in a different buffer formulation containing PBS, BSA and sodium azide (ab252848)
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Immunocytochemical analysis of 100% methanol-fixed HeLa (human cervix adenocarcinoma epithelial cell) cells labeling PCNA (green) using ab252848 at 7.08µg/ml followed by ab150157 Goat Anti-Rat IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (2µg/ml). ab179504 Anti-beta IV Tubulin antibody was used as a counterstain at 1/200 dilution (10µg/ml) followed by ab150080 AlexaFluor®594 Goat anti-Rabbit secondary at 1/1000 dilution (2µg/ml) (Red). Confocal image showing nuclear staining in HeLa cell line. The nuclear counterdstain was DAPI (Blue).
-ve control 1: ab252848 (1/50 dilution) followed by ab150080 (1/1000 dilution).
-ve control 2: ab179504 (1/200 dilution) followed by ab150157 (1/1000 dilution).
This image was produced by the same antibody in a different buffer formulation containing PBS, BSA and sodium azide (ab252848)
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