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CATEGORIES

Goat anti-Equine IgG

Product classification
Antibodies Purified Secondary Antibodies
Catalog No CAB.94027
Antibody overview
CAB.94027 Antibodies
Goat anti-Equine IgG
Ordering
Available Variants
3 Variants
Change View
1mg
SKU
CAB.94027-1mg
Price
€27.50
Available – Dispatch in 14 days
10mg
SKU
CAB.94027-10mg
Price
€1562.50
Available – Dispatch in 14 days
100mg
SKU
CAB.94027-100mg
Price
€1562.50
Available – Dispatch in 14 days
Availability & Stock Pack SKU Price (EUR)
Available – Dispatch in 14 days
Global Network - International delivery
1mg CAB.94027-1mg €27.50
Available – Dispatch in 14 days
Global Network - International delivery
10mg CAB.94027-10mg €1562.50
Available – Dispatch in 14 days
Global Network - International delivery
100mg CAB.94027-100mg €1562.50
Quick page guide: Compare pack sizes, review validated applications and access product documents from this section.
Recommended Dilution
WB 1:200-1000
Dilution ELISA:1:5000-50000
Validated Application Key
ELISA WB
Validated application
ELISA WB - Validated application
Technical Specifications
Catalog No CAB.94027
Product Name Goat anti-Equine IgG
Isotype IgG
Calculated MW 150kDa
Immunogen Equine IgG full length protein
Public Immunogen Range N/A
Host Goat
Clone Type Polyclonal Antibody
Reactivity Equine
Application ELISA WB
Subcellular Location N/A
Purification Method CABfinity purification
Storage Buffer Buffer: PBS with 0.03% Proclin300 (PH7.2-7.4).
Storage Shipped at 4℃, Store at -20℃ at least one year (Avoid repeated freeze/thaw cycles).

Background

Immunoglobulin G (IgG),is one of the most abundant proteins in serum with normal levels between 8-17 mg/mL in blood. IgG is important for our defence against microorganisms and the molecules are produced by B lymphocytes as a part of our adaptive immune response. The IgG molecule has two separate functions;to bind to the pathogen that elicited the response and to recruit other cells and molecules to destroy the antigen. The variability of the IgG pool is generated by somatic recombination and the number of specificities in an individual at a given time point is estimated to be 1011 variants.

Protocol / Instructions

Recommended workflow
Optimized handling and experimental guidance
Review the suggested sequence below before starting the assay to keep sample handling, incubation, and downstream interpretation aligned.
Lab-ready steps

The Goat anti-Equine IgG antibody is designed for use in various applications including ELISA and Western Blotting.

## ELISA Protocol

For ELISA, the recommended dilution is 1:5000-50000. Reagents and buffers required include a 96-well plate, antigen, blocking buffer, and substrate. Sample preparation involves coating the plate with antigen and blocking non-specific binding sites. Antibody incubation is performed by adding the Goat anti-Equine IgG antibody at the recommended dilution, followed by washing and detection using a secondary antibody conjugated to an enzyme. Technical notes: Optimize the antibody dilution and incubation time to achieve the best results.

## Western Blotting Protocol

For Western Blotting, the recommended dilution is 1:200-1000. Reagents and buffers required include a transfer membrane, blocking buffer, and substrate. Sample preparation involves separating proteins by SDS-PAGE and transferring them to a membrane. Antibody incubation is performed by adding the Goat anti-Equine IgG antibody at the recommended dilution, followed by washing and detection using a secondary antibody conjugated to an enzyme. Technical notes: Use a suitable positive control to verify the specificity of the antibody and optimize the blocking conditions to reduce non-specific binding.

**ELISA WB Protocol**

Use assay conditions validated for ELISA WB, apply Goat anti-Equine IgG at the recommended working dilution, include proper positive and negative controls, perform thorough wash steps, and document incubation time, temperature, and detection conditions for reproducible performance. Recommended dilution: WB 1:200-1000.;ELISA:1:5000-50000..

Precautions

Store at -20°C, handle with care, use appropriate controls, and optimize antibody dilution and incubation time for best results.

Validation Images

Goat anti-Equine IgG Figure 1
Fig.1. Validation data.