PARP10 Antibody - BSA Free

Novus Biologicals | Catalog # NB100-2157

Novus Biologicals
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Key Product Details

Validated by

Independent Antibodies

Species Reactivity

Validated:

Human

Cited:

Human

Applications

Validated:

Immunohistochemistry, Immunohistochemistry-Paraffin, Western Blot, Immunoprecipitation

Cited:

Western Blot, Knockdown Validated

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Format

BSA Free
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Product Specifications

Immunogen

The immunogen recognized by this antibody maps to a region between residue 300 and 350 of Poly (ADP-ribose) Polymerase Family, member 10 using the numbering given in entry NP_116178.1 (GeneID 84875)

Localization

Nuclear

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Scientific Data Images for PARP10 Antibody - BSA Free

Western Blot: PARP10 Antibody [NB100-2157]

Western Blot: PARP10 Antibody [NB100-2157]

Western Blot: PARP10 Antibody [NB100-2157] - Detection of Human PARP10 on HeLa whole cell lysate using NB100-2157. PARP10 was also immunoprecipitated using other rabbit anti-PARP10 antibodies.
Immunohistochemistry-Paraffin: PARP10 Antibody [NB100-2157]

Immunohistochemistry-Paraffin: PARP10 Antibody [NB100-2157]

Immunohistochemistry-Paraffin: PARP10 Antibody [NB100-2157] - Human ovarian carcinoma. Antibody: Affinity purified rabbit anti- PARP10 used at a dilution of 1:1,000 (1ug/ml). Detection: DAB
PARP10 Antibody - BSA Free

Western Blot: PARP10 Antibody - BSA Free [NB100-2157] -

Identification of genes necessary for proliferation of PARP10-overexpressing MCF10A breast epithelial cells by CRISPR-mediated genome-wide loss-of-function screening.(A) Western blot showing doxycycline-induced overexpression of PARP10 in MCF10A cells. (B) Overview of the CRISPR knockout screens to identify genes that are specifically required for proliferation of PARP10-overexpressing MCF10A cells. (C) Scatterplot showing the results of genome-wide CRISPR knockout screens to identify genes that are specifically required for proliferation of PARP10-overexpressing MCF10A cells. Each gene targeted by the library was ranked according to the MAGeCK score indicating genes which, when inactivated, specifically cause reduced proliferation in PARP10-overexpressing MCF10A-TREPARP10 cells compared to control MCF10A cells. Top hits chosen for validation are indicated. (D, E) Biological pathway analyses using KEGG (D) or Gene Ontology (E) analyses of the top hits with p-values lower than 0.02 which specifically cause reduced proliferation in PARP10-overexpressing MCF10A-TREPARP10 cells compared to control MCF10A cells. KEGG terms with negative logP greater than 1 are shown. GO_BP terms with negative logP greater than 1.24 are presented (corresponding to the top 20 pathways). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36187556), licensed under a CC-BY license. Not internally tested by Novus Biologicals.
PARP10 Antibody - BSA Free

Western Blot: PARP10 Antibody - BSA Free [NB100-2157] -

Functional interaction between ATM and PARP10 expression.(A) Western blot showing overexpression of PARP10 in two independent HeLa PARP10 CRISPRa cell lines. (B) CellTiterGlo cellular proliferation assays showing that knockdown of ATM, using two separate siRNA oligonucleotides, specifically reduces the proliferation of two different PARP10-overexpressing CRISPRa HeLa cell lines compared to control HeLa cells. The average of three experiments is shown (normalized to control siRNA). Error bars represent standard deviations, and asterisks indicate statistical significance (t-test, two-tailed, unpaired). (C) DNA fiber combing assays showing that ATM depletion does not differentially impact replication fork progression in PARP10-overexpressing CRISPRa HeLa cell lines compared to control HeLa cells. Replication tracts labeled by both IdU and CldU, indicating ongoing replication forks, were quantified, and their labeled tract length (IdU+CldU) is presented, with the median values marked on the graph and listed at the top. At least 60 tracts were quantified for each sample. Asterisks indicate statistical significance (Mann-Whitney test). A schematic representation of the assay conditions is shown at the top. (D–F) ATM SIRF experiments showing that PARP10 overexpression in HeLa cells increases HU-induced ATM binding to nascent DNA. HeLa cells were treated with 4 mM HU for 3 hours. ATM depletion was used as control, to demonstrate the specificity of the SIRF signal. Representative micrographs (D) and quantifications (E, F) are shown. Bars indicate the mean values, error bars represent standard errors, and asterisks indicate statistical significance (t-test, two-tailed, unpaired). Schematic representations of the assay conditions are shown at the top. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36187556), licensed under a CC-BY license. Not internally tested by Novus Biologicals.

Applications for PARP10 Antibody - BSA Free

Application
Recommended Usage

Immunohistochemistry

1:500 -1:2000

Immunohistochemistry-Paraffin

1:500 -1:2000

Immunoprecipitation

1-4 ug/mg of lysate

Western Blot

1:500-1:2500
Application Notes
Epitope retrieval with citrate buffer pH6.0 is recommended for FFPE tissue sections.

Formulation, Preparation, and Storage

Purification

Immunogen affinity purified

Formulation

Tris-Citrate/Phosphate (pH 7.0 - 8.0)

Format

BSA Free

Preservative

0.09% Sodium Azide

Concentration

1.0 mg/ml

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at 4C. Do not freeze.

Background: PARP10

PARP10 is a member of the poly(ADP-ribose) polymerase (PARP) family involved in a variety of processes which includes DNA metabolism, the DNA damage response, transcription and the maintenance of genomic stability. Although each member of the PARP family exhibits poly(ADP-ribose) polymerase activity which catalyzes the attachment of ADP-ribose units from NAD+ to substrate proteins, the endogenous substrates of many of the family members, including PARP10, remain to be identified. Recent studies have shown that PARP10 is localized to the nucleoli and associates with RNA polymerase II. PARP10 is a substrate of and is activated by CDK2 and may serve an important function in cell proliferation. Alternate names for PARP10 include poly(ADP-ribose) polymerase 10, PARP-10, and FLJ14464.

Long Name

Protein mono-ADP-ribosyltransferase PARP10

Alternate Names

ARTD10, PARP-10

Entrez Gene IDs

84875 (Human)

Gene Symbol

PARP10

Additional PARP10 Products

Product Documents for PARP10 Antibody - BSA Free

Certificate of Analysis

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Product Specific Notices for PARP10 Antibody - BSA Free

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Citations for PARP10 Antibody - BSA Free

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Protocols

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