• Phare
  • Validé par KD/KO

Anticorps Polyclonal de lapin anti-PARD3

PARD3 Polyclonal Antibody for FC, IF, IHC, IP, WB, ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain, souris et plus (2)

Applications

WB, IP, IHC, IF, FC, CoIP, ELISA

Conjugaison

Non conjugué

N° de cat : 11085-1-AP

Synonymes

ASIP, Baz, Bazooka, CTCL tumor antigen se2 5, PAR 3, PAR3, PAR3 alpha, PAR3A, PAR3alpha, PARD 3, PARD3, PARD3A, SE2 5L16, SE2 5LT1, SE2 5T2



Applications testées

Résultats positifs en WBcellules A549, cellules HEK-293, cellules HeLa, cellules MCF-7
Résultats positifs en IPcellules MCF-7
Résultats positifs en IHCtissu de cancer du côlon humain,
il est suggéré de démasquer l'antigène avec un tampon de TE buffer pH 9.0; (*) À défaut, 'le démasquage de l'antigène peut être 'effectué avec un tampon citrate pH 6,0.
Résultats positifs en IFcellules MCF-7, tissu cérébral de souris, tissu rénal de souris
Résultats positifs en cytométriecellules MCF-7

Dilution recommandée

ApplicationDilution
Western Blot (WB)WB : 1:2000-1:10000
Immunoprécipitation (IP)IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
Immunohistochimie (IHC)IHC : 1:50-1:200
Immunofluorescence (IF)IF : 1:200-1:800
Flow Cytometry (FC)FC : 0.20 ug per 10^6 cells in a 100 µl suspension
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, check data in validation data gallery

Informations sur le produit

11085-1-AP cible PARD3 dans les applications de WB, IP, IHC, IF, FC, CoIP, ELISA et montre une réactivité avec des échantillons Humain, souris

Réactivité Humain, souris
Réactivité citéerat, Humain, poulet, souris
Hôte / Isotype Lapin / IgG
Clonalité Polyclonal
Type Anticorps
Immunogène PARD3 Protéine recombinante Ag1565
Nom complet par-3 partitioning defective 3 homolog (C. elegans)
Masse moléculaire calculée 151 kDa
Poids moléculaire observé 180 kDa, 140-150 kDa, 100 kDa
Numéro d’acquisition GenBankBC011711
Symbole du gène PARD3
Identification du gène (NCBI) 56288
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par affinité contre l'antigène
Tampon de stockage PBS avec azoture de sodium à 0,02 % et glycérol à 50 % pH 7,3
Conditions de stockageStocker à -20°C. Stable pendant un an après l'expédition. L'aliquotage n'est pas nécessaire pour le stockage à -20oC Les 20ul contiennent 0,1% de BSA.

Informations générales

PARD3 (also known as ASIP, Par3, or Bazooka) is one of PARD proteins which are essential for asymmetric cell division and polarized growth. PARD3 is involved in the establishment of cell polarity and in the asymmetric cytokinesis. It plays a role in tight junctions at epithelial cell-cell contacts. PARD3 has three splice isoforms at 100 kDa, 150 kDa, and 180 kDa. This polyclonal antibody raised against C-terminal 281 amino acids of human PARD3 recognizes these three isoforms.

Protocole

Product Specific Protocols
WB protocol for PARD3 antibody 11085-1-APDownload protocol
IHC protocol for PARD3 antibody 11085-1-APDownload protocol
IF protocol for PARD3 antibody 11085-1-APDownload protocol
IP protocol for PARD3 antibody 11085-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
mouseIF

Nat Commun

EMX2-GPR156-Gαi reverses hair cell orientation in mechanosensory epithelia.

Authors - Katie S Kindt
mouseIF

Matrix Biol

Ameloblastin promotes polarization of ameloblast cell lines in a 3-D cell culture system

Authors - Gayathri Visakan
chickenIHC,IF

Development

Coupling of apical-basal polarity and PCP to interpret the Wnt signaling gradient and orient feather branch.

Authors - Jianqiong Lin
  • KD Validated

FASEB J

Perturbation of epithelial apicobasal polarity by rhomboid family-1 gene overexpression.

Authors - Xue-Mei Peng
mouseWB

iScience

Glucocorticoid receptor-mediated Nr1d1 chromatin circadian misalignment in stress-induced irritable bowel syndrome

Authors - Gen Zheng
mouseIP

Front Cell Dev Biol

Nox1-based NADPH oxidase regulates the Par protein complex activity to control cell polarization

Authors - Alejandra Valdivia

Avis

The reviews below have been submitted by verified Proteintech customers who received an incentive forproviding their feedback.


FH

Sarah (Verified Customer) (06-26-2019)

Western blot: Total cell lysate (15 ug) was resolved on a 4-12% Bis-Tris gel and transferred to nitrocellulose membrane. Membrane was incubated in blocking buffer (5% milk/0.1% Tween-20) for 1h. Membrane was incubated with anti-PARD-3 in blocking buffer (1:1000) at 4C overnight. After washing, membrane was incubated in anti-rabbit-HRP in blocking bufffer (1:3000) for 1h at room temperature. Protein was detected using ECL reagent and imaged on a chemiluminescence detection system.Immunofluorescence: Cells fixed in MeOH at -20 degrees were stained with 1:200 primary antibody. After washing, coverslips were incubated in 1:500 AF488 secondary antibody. Following mounting, images were acquired using a confocal microscope. Staining was very weak, as is seen by the image (Green = PARD3, Blue = Hoescht)

  • Applications: Western Blot, Immunofluorescence,
  • Primary Antibody Dilution: 1:1000 (WB), 1:200 (IF)
  • Cell Tissue Type: MCF10A
PARD3 Antibody Western Blot,Immunofluorescence, validation (1:1000 (WB), 1:200 (IF) dilution) in MCF10A (Cat no:11085-1-AP)