Monoclonal Anti-Proliferating Cell Nuclear Antigen antibody produced in mouse, clone PC 10, ascites fluid

Code: P8825-.2ML D2-231

Application

Monoclonal Anti-Proliferating Cell Nuclear Antigen antibody produced in mouse has been used in: enzyme linked immuno sorbent assay (ELISA) immunoblotting immunohi...


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Application

Monoclonal Anti-Proliferating Cell Nuclear Antigen antibody produced in mouse has been used in: enzyme linked immuno sorbent assay (ELISA) immunoblotting immunohistology immunoprecipitation flow cytometry

Monoclonal Anti-Proliferating Cell Nuclear Antigen antibody produced in mouse has been used for immunohistochemistry (IHC) Western blotting (WB).

Biochem/physiol Actions

Proliferating cell nuclear antigen (PCNA) is essential for DNA replication during S-phase. It is essential for cellular DNA synthesis. PCNA is required for leading strand synthesis in the SV40 system where it acts as an auxiliary protein for polymerase.

PCNA (proliferating cell nuclear antigen) is loaded around the template-primer 3′ ends, which is recognized by the conserved chaperone-like complex RFC (replication factor C), and this mechanism is ATP-dependent. Encircling of the DNA by the PCNA ring ensures firm anchoring of the polymerases to the DNA, and hence, functions as a co-factor for DNA polymerases. Post-translation modifications of this protein at the K164 residue is required for the regulation of DNA damage tolerance (DDT) pathways, pathways that ensure recovery from replication arrest at DNA lesions.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

General description

Monoclonal Anti-Proliferating Cell Nuclear Antigen (mouse IgG2a isotype) is derived from the PC 10 hybridoma produced by the fusion of mouse myeloma cells and splenocytes from a BALB/c mouse immunized with PCNA-Protein A fusion protein. Proliferating cell nuclear antigen (PCNA, 36 kDa), also known as cyclin, is an auxiliary protein of DNA polymerase. The protein is present in the nucleoplasm of continually cycling cells throughout the cell cycle.

PCNA (proliferating cell nuclear antigen) is a member of the structurally and functionally conserved family of DNA sliding clamps (β clamps). They exist as ring-shaped complexes- homotrimers in eukaryotes, having pseudohexameric symmetry. A monomer of PCNA is composed of two similar globular domains, connected by an interdomain connecting loop, which is a long, and probably a flexible loop. These monomers organize themselves in a head-to-tail manner to form a ring, which has an inner positively charged surface composed of α helices and an outer surface of β sheets.

Immunogen

PCNA-Protein A fusion protein

Specificity

Recognizes the acidic, non-histone, auxiliary protein of DNA polymerase, PCNA, also known as polymerase delta accessory protein. Fixation duration can markedly affect the intensity of PCNA immunoreactivity. However, delay in fixation does not affect the immunoreactivity. Enzymatic treatment destroys staining. In immunocytochemical labeling of acetone-methanol, or methanol-fixed cells, the antibody shows granular staining throughout the nucleus (nucleolus and nucleoplasm). Specific staining is observed in proliferating cell nuclei, particularly in germinal centers, of a wide range of normal and malignant tissues.

antibody formascites fluid
antibody product typeprimary antibodies
biological sourcemouse
clonePC 10, monoclonal
conjugateunconjugated
contains15 mM sodium azide
Gene Informationhuman ... PCNA(5111)
isotypeIgG2a
packagingantibody small pack of 25 µL
Quality Level200
shipped indry ice
species reactivityrat, mouse, yeast, monkey, insect, human
storage temp.−20°C
technique(s)indirect ELISA: suitable, immunocytochemistry: suitable, immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:3,000 using human tonsil sections, microarray: suitable, flow cytometry: suitable, immunoprecipitation (IP): suitable, western blot: 1:3,000 using HS-68 human foreskin- cell extract, immunohistochemistry (frozen sections): suitable
UniProt accession no.P12004, P04961
This product has met the following criteria to qualify for the following awards:



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