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Catalog Number Size Price
LS-C829620-100 100 µl $393 
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of rat kidney. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of rat kidney. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of rat testis. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of rat testis. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of rat testis. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of mouse kidney. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of mouse epididymis. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of mouse kidney. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of rat kidney. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of mouse kidney. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of rat kidney. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of rat kidney. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of rat testis. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of rat testis. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of rat testis. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of mouse kidney. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of mouse epididymis. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of mouse kidney. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of rat kidney. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
TJP1 / ZO-1 Antibody - IHC-P on paraffin sections of mouse kidney. The animal was perfused using Autoperfuser at a pressure of 130 mmHg with 300 ml 4% FA before being processed for paraffin embedding. HIER: Tris-EDTA, pH 9 for 20 min using Thermo PT Module. Blocking: 0.2% LFDM in TBST filtered through 0.2 µm. Detection was done using Novolink HRP polymer from Leica following manufacturers instructions; DAB chromogen: Candela DAB chromogen. Primary antibody: dilution 1:500, incubated 30 min at RT using Autostainer. Sections were counterstained with Harris Hematoxylin.
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Polyclonal Rabbit‑New Zealand White anti‑Mouse TJP1 / ZO‑1 Antibody (IHC, WB) LS‑C829620

Polyclonal Rabbit‑New Zealand White anti‑Mouse TJP1 / ZO‑1 Antibody (IHC, WB) LS‑C829620

Antibody:
TJP1 / ZO-1 Rabbit-New Zealand White anti-Mouse Polyclonal Antibody
Application:
IHC, WB
Reactivity:
Mouse, Rat
Format:
Unconjugated, Unmodified
Price
Catalog Number
$393
LS-C829620-100
Toll Free North America
(800) 227-6666
For Research Use Only

Overview

Antibody:
TJP1 / ZO-1 Rabbit-New Zealand White anti-Mouse Polyclonal Antibody
Application:
IHC, WB
Reactivity:
Mouse, Rat
Format:
Unconjugated, Unmodified

Specifications

Description
ZO-1 antibody LS-C829620 is an unconjugated rabbit-new zealand white polyclonal antibody to ZO-1 (TJP1) from mouse. It is reactive with mouse and rat. Validated for IHC and WB.
Target
Mouse TJP1 / ZO-1
Synonyms
TJP1 | ZO-1 | Zona occludens protein 1 | Zona occludens 1 | Zonula occludens protein 1 | Tight junction protein 1 | ZO1 | Tight junction protein ZO-1 | Zonula occludens 1 protein
Host
Rabbit-New Zealand White
Reactivity
Mouse, Rat (tested or 100% immunogen sequence identity)
Clonality
Polyclonal
Conjugations
Unconjugated
Modifications
Unmodified
Immunogen
A synthetic peptide from mouse ZO1 conjugated to blue carrier protein was used as the antigen. The peptide is homologous in rat.
Applications
  • IHC (1:500)
  • Western blot (1:500)
Performing IHC? See our complete line of Immunohistochemistry Reagents including antigen retrieval solutions, blocking agents ABC Detection Kits and polymers, biotinylated secondary antibodies, substrates and more.
Usage
Applications should be user optimized.
Presentation
Lyophilized. Whole Serum.
Reconstitution
Reconstitute in 100 ul of sterile water. Centrifuge to remove any insoluble material. Glycerol (1:1) may be added for an additional stability.
Storage
Store at 2°C to 8°C for short term storage, or at -20°C for long term storage. Stable for up to 12 months after reconstitution. Avoid freeze/thaw cycles.
Restrictions
For research use only. Intended for use by laboratory professionals.
Guarantee
This antibody carries the LSBio 100% Guarantee.
LSBio Guarantee
About TJP1 / ZO-1
Q07157 NM_003257 NP_003248.3

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Requested From: United States
Date Requested: 12/21/2024