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Home >> Antibodies >> PCNA Antibody

PCNA Antibody [clone PC10] (V2218)

  Catalog No Formulation Size Price (USD)  
Image V2218-100UG 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced) and 0.05% sodium azide 100 ug 519
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V2218-20UG 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced) and 0.05% sodium azide 20 ug 229
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V2218SAF-100UG 1 mg/ml in 1X PBS; BSA free, sodium azide free 100 ug 519
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V2218IHC-7ML Prediluted in 1X PBS with 0.1 mg/ml BSA (US sourced) and 0.05% sodium azide; *For IHC use only* 7 ml 519
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Western blot testing of HeLa cell lysate with PCNA antibody (clone PC10). Predicted molecular weight ~29 kDa, routinely observed at 29~36 kDa.
Flow cytometry staining of human A549 cells with PCNA antibody; Red=isotype control, Blue= PCNA antibody.
IHC testing of human human tonsil stained with PCNA antibody (PC10).
SDS-PAGE analysis of purified, BSA-free PCNA antibody (clone PC10) as confirmation of integrity and purity.
Species Reactivity Human, Mouse, Rat
Format Purified
Clonality Monoclonal (mouse origin)
Isotype Mouse IgG2a, kappa
Clone Name PC10
Purity Protein G affinity chromatography
Buffer 1X PBS, pH 7.4
Gene ID 5111
Localization Predominantly nuclear, some cytoplasmic
Applications Flow cytometry : 1-2ug/10^6 cells
Immunofluorescence : 0.5-1ug/ml
Western blot : 0.5-1ug/ml
Immunohistochemistry (FFPE) : 0.25-0.5ug/ml for 30 min at RT
Limitations This PCNA antibody is available for research use only.
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Description

This antibody recognizes a non-histone protein of 36 kDa, which is identified as proliferating cell nuclear antigen (PCNA). PCNA is also known as cyclin or polymerase delta auxiliary protein. Elevated expression of PCNA-cyclin has been shown in the nucleus during late G1 phase immediately before the onset of DNA synthesis, becoming maximal during S-phase and declining during G2 and M phases. This antibody is excellent for the detection of PCNA in multiple applications.

Application Notes

The concentration stated for each application is a general starting point. Variations in protocols, secondaries and substrates may require the antibody to be titered up or down for optimal performance.

1. Staining of formalin-fixed tissues requires boiling tissue sections in 10mM citrate buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minutes.
2. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.

Immunogen

Rat PCNA / Protein A fusion protein was used as the immunogen for this antibody.

Storage

Store the PCNA antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).

Alternate Names

Cyclin; Mutagen-sensitive 209 protein; PCNAR; Polymerase delta accessory protein, PCNA antibody

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