Human PARD3/Par3 Antibody Summary
Tyr451-Glu555
Accession # Q8TEW0
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
PARD3/Par3 in HEK293 Human Cell Line. PARD3/Par3 was detected in immersion fixed HEK293 human embryonic kidney cell line using Mouse Anti-Human PARD3/Par3 Monoclonal Antibody (Catalog # MAB8030) at 25 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Mouse IgG Secondary Antibody (red; Catalog # NL007) and counterstained with DAPI (blue). Specific staining was localized to plasma membrane. View our protocol for Fluorescent ICC Staining of Cells on Coverslips.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: PARD3/Par3
PARD3 (partitioning defective 3 homolog), also called Par3, is a widely expressed adapter protein involved in asymmetrical cell division, cell polarization, and tight junction formation. It forms a cell polarity complex with Par6 and aPKC (atypical protein kinase C), linking to PTEN (phosphatase and tensin homolog) in polarized epithelia and VE-Cadherin in polarized endothelia. The region used as an immunogen, human PARD3 amino acids (aa) 451-555 (of 1356 aa in full-length PARD3) shares 97% and 96% aa sequence identity with mouse and rat PARD3, respectively. It includes the second of three PDZ domains, a region which is involved in heterophilic interactions and is present within all 10 reported PARD3 isoforms that vary in length from 988 aa to 1356 aa.
Product Datasheets
Citations for Human PARD3/Par3 Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 2
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DAPLE orchestrates apical actomyosin assembly from junctional polarity complexes
Authors: Arthur Marivin, Rachel Xi-Yeen Ho, Mikel Garcia-Marcos
Journal of Cell Biology
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Hypoxia disrupt tight junctions and promote metastasis of oral squamous cell carcinoma via loss of par3
Authors: S Kim, S Park, EH Moon, GJ Kim, J Choi
Cancer Cell International, 2023-04-24;23(1):79.
Species: Human
Sample Types: Cell Lysates, Whole Cells, Whole Tissues
Applications: Western Blot, ICC, IHC
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