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Purified anti-γ-Catenin Antibody

Pricing & Availability
Clone
W22004E (See other available formats)
Regulatory Status
RUO
Other Names
Catenin gamma, Desmoplakin III, desmoplakin-3, DP3CTNNG, DPIII, gamma-catenin, junction plakoglobin, PDGBARVD12, PKGB, JUP, dp3, Catenin (Cadherin-associated Protein), Gamma 80kDa, CTNNG, PDGB, Desmoplakin 3
Isotype
Rat IgG2b, κ
Ave. Rating
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Product Citations
publications
A. W22004E_PURE_WB_Ab_091323
Whole cell extracts (15 µg total protein per lane) from the indicated cell lines were resolved on a 4-12% Bis-Tris gel, transferred to a PVDF membrane, and probed with 1 µg/mL of purified anti-γ-Catenin (clone W22004E) overnight at 4°C. Proteins were visualized by chemiluminescence detection using HRP Goat anti-rat IgG (Cat. No. 405405) at a 1:5000 dilution. Direct-Blot™ HRP anti-β-actin (Cat. No. 664804) was used as a loading control at a 1:25000 dilution. Western-Ready™ ECL Substrate Premium Kit (Cat. No. 426319) was used as a detection reagent. Lane M: Molecular weight marker
  • A. W22004E_PURE_WB_Ab_091323
    Whole cell extracts (15 µg total protein per lane) from the indicated cell lines were resolved on a 4-12% Bis-Tris gel, transferred to a PVDF membrane, and probed with 1 µg/mL of purified anti-γ-Catenin (clone W22004E) overnight at 4°C. Proteins were visualized by chemiluminescence detection using HRP Goat anti-rat IgG (Cat. No. 405405) at a 1:5000 dilution. Direct-Blot™ HRP anti-β-actin (Cat. No. 664804) was used as a loading control at a 1:25000 dilution. Western-Ready™ ECL Substrate Premium Kit (Cat. No. 426319) was used as a detection reagent. Lane M: Molecular weight marker
  • B. W22004E_PURE_IHC-P_091323
    IHC staining using purified anti-γ-Catenin (clone W22004E) on formalin-fixed paraffin-embedded human colon tissue. Following antigen retrieval using 1X Citrate buffer (Cat. No. 420901), the tissue was incubated with 5 µg/mL of purified anti-γ-Catenin (clone W22004E) overnight at 4°C, followed by incubation with 2.5 µg/mL of Alexa Fluor® 647 Goat anti-rat IgG (red) (Cat. No. 405416) for one hour at room temperature. Nuclei were counterstained with DAPI (blue) (Cat. No. 422801). The image was captured with a 40X objective. Scale bar: 50 µM
  • C. W22004E_PURE_IHCP_091323
    IHC staining using purified anti-γ-Catenin (clone W22004E) on formalin-fixed paraffin-embedded human skin tissue. Following antigen retrieval using 1X Citrate buffer (Cat. No. 420901), the tissue was incubated with 1 µg/mL of purified anti-γ-Catenin (clone W22004E) overnight at 4°C, followed by incubation with 2.5 µg/mL of Alexa Fluor® 647 goat anti-rat IgG (red) (Cat. No. 405416) for one hour at room temperature. Nuclei were counterstained with DAPI (blue) (Cat. No. 422801). The image was captured with a 40X objective. Scale bar: 50 µM
  • D. W22004E_PURE_ICC_091323
    HaCat cells were fixed with 4% paraformaldehyde for 10 minutes, permeabilized with 0.5% Triton X-100, and blocked with 5% FBS for 1 hour at room temperature. Cells were then intracellularly stained with 5.0 µg/mL of purified anti-γ-Catenin (clone W22004E), followed by incubation with 2.5 µg/mL of Alexa Fluor® 488 Goat anti-rat IgG (Cat. No. 405418) for 1 hour at room temperature (panel A). Nuclei were counterstained with DAPI (Cat. No. 422801) and F-actin was counterstain with Flash Phalloidin™ Red 594 (Cat. No. 424203) (panel B). The image was captured with a 40X objective. Scale bar: 25 µm
  • E. W22004E_PURE_ICFC_091323
    HaCaT cells were fixed and permeabilized with Cyto-Fast™ Fix/Perm Buffer set (Cat. No. 426803). Then cells were intracellularly stained with purified anti-γ-Catenin (clone W22004E) (filled histogram) or purified rat IgG2b, κ isotype control (open histogram, dashed line) (Cat. No. 400602), followed by APC Goat anti-rat IgG (Cat. No. 405407).
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624051 25 µg £130
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624052 100 µg £322
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Description

γ-Catenin, also called plakoglobin or JUP, is a member of the armadillo family of signaling molecules. γ-Catenin plays an important role in cell adhesion with α-catenin and β-catenin, participates in Wnt signaling, embryonic development and tumorigenesis. Though β-catenin and γ-Catenin share sequence homology, γ-catenin has distinct N- and C-terminal regions which imparts distinct functions through interaction with various protein partners. Recent evidence indicates that γ-Catenin modulates desmosomal adhesion in response to growth factor stimulation. Transgenic mice homozygous with a null mutation of the γ-Catenin gene die during the embryonic stage, approximately on the 12th day of development, due to significant abnormalities in the adherens junctions and the absence of properly functioning desmosomes in the heart. The alteration of the γ-Catenin gene has been suggested as a contributing factor in the development of the heart disease called arrhythmogenic right ventricular dysplasia (ARVD) or arrhythmogenic right ventricular cardiomyopathy. Specifically, the mutations in γ-Catenin result in an autosomal recessive type of the disease known as Naxos disease.

Product Details
Technical Data Sheet (pdf)

Product Details

Verified Reactivity
Human, Mouse
Antibody Type
Monoclonal
Host Species
Rat
Immunogen
Partial Recombinant human γ-Catenin protein
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide
Preparation
The antibody was purified by affinity chromatography.
Concentration
0.5 mg/mL
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C.
Application

WB - Quality tested
IHC-P, ICC, ICFC - Verified
Recommended Usage

Each lot of this antibody is quality control tested by western blotting. For western blotting, the suggested use of this reagent is 0.125 - 1.0 µg/mL. For immunohistochemistry on formalin-fixed paraffin-embedded tissue sections, a concentration range of 1.0 - 10.0 µg/mL is suggested. For immunocytochemistry, a concentration range of 1.0 - 5.0 μg/mL is recommended. For flow cytometric staining, the suggested use of this reagent is ≤ 0.06 µg per million cells in 100 µL volume. It is recommended that the reagent be titrated for optimal performance for each application. 

Application Notes

This clone cross-reacts with mouse γ-Catenin.

For immunocytochemistry (ICC), the suggested fixation/permeabilization method is either 4% paraformaldehyde/0.5% Triton X-100 or paraformaldehyde followed by ice-cold methanol or fixed with ice-cold methanol only.

For immunohistochemistry (IHC-P), the suggested antigen retrieval buffer is Citrate Buffer (Cat. No. 420901) or Tris-EDTA pH 9.0.

For ICFC (intracellular flow cytometry) staining with this clone, we recommended using Cyto-Fast™ Fix/Perm Buffer Set (Cat. No. 426803) or True-Nuclear™ Transcription Factor Buffer Set (Cat. No. 424401). True-Phos™ Perm Buffer (Cat. No. 425401) and Intracellular Staining Permeabilization Wash Buffer (Cat. No. 421002) are not applicable.

RRID
AB_3097234 (BioLegend Cat. No. 624051)
AB_3097234 (BioLegend Cat. No. 624052)

Antigen Details

Structure
γ-Catenin is a 745 amino acid protein with a predicted molecular weight of 82 kD
Distribution

Cardiac cells

Function
Regulation of cell-cell adhesion
Interaction
MUC1, CAV1, PTPRJ, DSG1, DSC1, DSC2, PKP2
Biology Area
Cell Adhesion, Cell Biology, Cell Motility/Cytoskeleton/Structure, Signal Transduction
Antigen References
  1. Zhurinsky J, et al. 2000. J Cell Sci. 113:3127-39.
  2. Zhurinsky J, et al. 2000. Mol Cell Biol. 20:4238-53.
  3. Charpentier E, et al. 2000. J Cell Biol. 149:503-20.
  4. Kolligs FT, et al. 2000. Genes Dev. 14:1319-31.
  5. Yin T, et al. 2005. J Biol Chem. 280:40355-63.
  6. Ruiz P, et al. 1996. J Cell Biol. 135:215-25.
  7. Bierkamp C, et al. 1996. Dev Biol. 180:780-85.
  8. Zhang Z. et al. 2015. J Clin Invest. 125:1708-12.
  9. Li D. et al. 2015. J Biol Chem. 287:10435-43.
  10. Rampazzo A. 2006. Heart Int. 2:17.
Gene ID
3728 View all products for this Gene ID
UniProt
View information about γ-Catenin on UniProt.org

Related FAQs

There are no FAQs for this product.
Go To Top Version: 1    Revision Date: 09/13/2023

For Research Use Only. Not for diagnostic or therapeutic use.

 

This product is supplied subject to the terms and conditions, including the limited license, located at www.biolegend.com/terms) ("Terms") and may be used only as provided in the Terms. Without limiting the foregoing, BioLegend products may not be used for any Commercial Purpose as defined in the Terms, resold in any form, used in manufacturing, or reverse engineered, sequenced, or otherwise studied or used to learn its design or composition without express written approval of BioLegend. Regardless of the information given in this document, user is solely responsible for determining any license requirements necessary for user’s intended use and assumes all risk and liability arising from use of the product. BioLegend is not responsible for patent infringement or any other risks or liabilities whatsoever resulting from the use of its products.

 

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This data display is provided for general comparisons between formats.
Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors.
If you need assistance with selecting the best format contact our expert technical support team.

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