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25% off all ELISA kits

Use code ELISA25-262 for 25% off all ELISAs through November.

S-Nitrosylated ACE-2 ELISA Kit

Measures s-nitrosylated ACE-2 and total ACE-2 in human cell and tissue lysates, enabling precise assessment of ACE-2 s-nitrosylation by ELISA.

This assay can be developed for other species (mouse, rat, etc.) upon request. Contact techsupport@raybiotech.com.

Product Description

Specifications

Size	1 Plate Kit, 2 Plate Kit, 5 Plate Kit
Estimated Lead Time	4-8 weeks
Species	Human
Compatible Sample Types	Tissue Lysates, Cell Lysates
Accession Number	Q9BYF1
Gene Id	59272
Gene Symbols	ACE2, UNQ868/PRO1885
Protein Name / Synonyms	Angiotensin-converting enzyme 2; Angiotensin-converting enzyme homolog (ACEH); Angiotensin-converting enzyme-related carboxypeptidase (ACE-related carboxypeptidase); Metalloprotease MPROT15
Solid Support	96-well Microplate
Design Principle	Sandwich-based
Method Of Detection	Colorimetric
Research Area	Post-Translational Modifications, Nitrosylation, Epigenetics
Modification	S-Nitrosylation
Shipping Type	Blue ice
Storage	-20°C

Introduction

The RayBio^® S-Nitrosylated-ACE-2 ELISA Kit uses a modified "biotin-switch" method to allow for the direct visualization of human S-Nitrosylated ACE-2 by ELISA. In this S-Nitrosylation biotin switch assay, unmodified free cysteines are first blocked. S-Nitrosylated cysteines are then selectively reduced for specific labeling with biotin-maleimide reagents, which irreversibly bind to the cysteine thiol that was S-Nitrosylated. Biotinylation of the newly formed thiol groups can then be detected by ELISA. An anti-pan ACE-2 antibody has been coated onto a 96-well plate. Biotinylated samples are pipetted into the wells and ACE-2 present in a sample is bound to the wells by the immobilized antibody. The wells are washed and HRP-conjugated streptavidin is used to detect S-Nitrosylated ACE-2. The wells are again washed, a TMB substrate solution is added to the wells and color develops in proportion to the amount of S-Nitrosylated ACE-2 bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.

Product Features

Quantify quickly and easily
Screen numerous different lysates without performing a Western Blot analysis
Minimal hands-on time, convenient, and non-radioactive material

Kit Components

Component	Size / Qty
Microplate Coated With Anti-Pan-ACE-2 Antibody	1 plate
Positive Control	1 vial
HRP-Conjugated Streptavidin	200 μL
Wash Buffer	25 mL
Assay Diluent	15 mL
Lysis Buffer	5 mL
TMB One-Step Substrate Reagent	12 mL
Stop Solution	8 mL
S-Nitrosylation Buffer A	12 mL
S-Nitrosylation Buffer B	3 mL
S-Nitrosylation Buffer C	5 mL
S-Nitrosylation Buffer D	3 mL
S-Nitrosylation Buffer E	12 mL
S-Nitrosylation Blocking Reagent	2 vials
S-Nitrosylation Reduction Reagent I	2 vials
S-Nitrosylation Reduction Reagent II	2 vials
S-Nitrosylation Labeling Reagent	2 vials

Additional Materials Required

Acetone (pre-chilled (-20°C))
Microplate reader capable of measuring absorbance at 450 nm
Protease and Phosphatase inhibitors
Precision pipettes to deliver 2 μL to 1 mL volumes
Adjustable 1-25 mL pipettes for reagent preparation
100 mL and 1 liter graduated cylinders
Log-log graph paper or computer and software for ELISA data analysis
Absorbent paper
Tubes to prepare positive control or sample dilutions
Distilled or deionized water
Shaker

Assay Procedure Summary

Prepare all reagents, samples and Positive Control as instructed.
Block unmodified free cysteines using prepared S-Nitrosylation Blocking Buffer at 50°C with gentle rocking.
Precipitate proteins with ice-cold acetone.
Wash protein pellet twice with cold acetone/water mixture.
Resuspend protein pellets in Buffers and adding Reducing and Labeling Reagents.
Precipitate proteins with ice-cold acetone.
Resuspend protein pellets.
Add 100 μL sample and Positive Control to each well. Incubate 2.5 hours at room temperature or overnight at 4°C with gentle shaking.
Add 100 μL prepared HRP-Conjugated Streptavidin solution. Incubate for 1 hour at room temperature with gentle shaking.
Add 100 μL TMB One-Step Substrate Reagent to each well. Incubate 30 minutes at room temperature.
Add 50 μL Stop Solution to each well. Read at 450 nm immediately.

Storage/Stability

The entire kit may be stored at -20°C for up to 6 months from the date of shipment. Avoid repeated freeze-thaw cycles.

Customization

This assay can be developed for other species (mouse, rat, etc.) upon request. Contact techsupport@raybiotech.com for more information.

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Introduction

Product Features

Quantify quickly and easily
Screen numerous different lysates without performing a Western Blot analysis
Minimal hands-on time, convenient, and non-radioactive material

Kit Components

Component	Size / Qty
Microplate Coated With Anti-Pan-ACE-2 Antibody	1 plate
Positive Control	1 vial
HRP-Conjugated Streptavidin	200 μL
Wash Buffer	25 mL
Assay Diluent	15 mL
Lysis Buffer	5 mL
TMB One-Step Substrate Reagent	12 mL
Stop Solution	8 mL
S-Nitrosylation Buffer A	12 mL
S-Nitrosylation Buffer B	3 mL
S-Nitrosylation Buffer C	5 mL
S-Nitrosylation Buffer D	3 mL
S-Nitrosylation Buffer E	12 mL
S-Nitrosylation Blocking Reagent	2 vials
S-Nitrosylation Reduction Reagent I	2 vials
S-Nitrosylation Reduction Reagent II	2 vials
S-Nitrosylation Labeling Reagent	2 vials

Additional Materials Required

Acetone (pre-chilled (-20°C))
Microplate reader capable of measuring absorbance at 450 nm
Protease and Phosphatase inhibitors
Precision pipettes to deliver 2 μL to 1 mL volumes
Adjustable 1-25 mL pipettes for reagent preparation
100 mL and 1 liter graduated cylinders
Log-log graph paper or computer and software for ELISA data analysis
Absorbent paper
Tubes to prepare positive control or sample dilutions
Distilled or deionized water
Shaker

Assay Procedure Summary

Prepare all reagents, samples and Positive Control as instructed.
Block unmodified free cysteines using prepared S-Nitrosylation Blocking Buffer at 50°C with gentle rocking.
Precipitate proteins with ice-cold acetone.
Wash protein pellet twice with cold acetone/water mixture.
Resuspend protein pellets in Buffers and adding Reducing and Labeling Reagents.
Precipitate proteins with ice-cold acetone.
Resuspend protein pellets.
Add 100 μL sample and Positive Control to each well. Incubate 2.5 hours at room temperature or overnight at 4°C with gentle shaking.
Add 100 μL prepared HRP-Conjugated Streptavidin solution. Incubate for 1 hour at room temperature with gentle shaking.
Add 100 μL TMB One-Step Substrate Reagent to each well. Incubate 30 minutes at room temperature.
Add 50 μL Stop Solution to each well. Read at 450 nm immediately.

Storage/Stability

The entire kit may be stored at -20°C for up to 6 months from the date of shipment. Avoid repeated freeze-thaw cycles.

Customization

This assay can be developed for other species (mouse, rat, etc.) upon request. Contact techsupport@raybiotech.com for more information.

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25% off all ELISA kits

25% off all ELISA kits

S-Nitrosylated ACE-2 ELISA Kit