At AAA Biotech, we provide a vast collection of high-quality, purified, conjugated and unconjugated secondary antibodies to use in various applications, such as Western Blotting, Flow Cytometry, Cell Imaging, or CUT & Tag.
Our secondary antibodies are available with a wide range of labels—such as HRP, AP, FITC, and biotin—to match your detection system and enhance signal sensitivity. Each antibody is rigorously tested to ensure high specificity and minimal cross-reactivity, delivering reliable performance across multiple species and assay types.
Whether you're conducting qualitative imaging or quantitative analysis, AAA Biotech has the right secondary antibody to support your research with consistency and precision. Our entire catalog of secondary antibodies is available for browsing through our main website.
Application Data (Rabbit peripheral blood lymphocytes were stained with Goat Anti-Rabbit IgG(H+L), Human ads-FITC)
FLISA (FLISA plate was coated with purified rabbit IgG and IgM. Immunoglobulins were detected with serially diluted Goat Anti-Rabbit IgG(H+L), Human ads-FITC)
IF (Immunofluorescence) (Immunofluorescence - anti-mCherry Ab (AB9770) using hCEC cells transduced with mCherry-Rab5a; cells were fixed with methanol and mCherry Ab at 1/250; 2nd Ab goat anti-IgY (AB307405) at 1:1,000;)
IF (Immunofluorescence) (Immunofluorescence -Anti-mCherry Ab (AB9770) using hCEC cells transduced with mCherry-Rab5a; cells were fixed with methanol and mCherry Ab at 1/250; 2nd Ab goatAnti-IgY (AB307405) at 1:1,000;)
WB (Western Blot) (Detection of GAPDH and hnRNP in HeLa Whole Cell Lysate. Primary Antibodies: cocktail of goat anti-GAPDH and mouse anti-hnRNP at 1 ug/ml each. Secondary Antibodies: cocktail of Dylight 680-conjugated rabbit anti-goat (red) and Dylight 488-conjugated rabbit anti-mouse AAA213715 (AAA213715-3) (blue) at 0.5 ug/ml each. Acquisition: Syngene G:Box, 39 seconds (red) and 60 seconds (blue).)
IF (Immunofluorescence) (Detection of human p53 by immunofluorescence. Sample: FFPE section of human breast carcinoma. Primary Antibody: mouse anti-p53 (clone DO-1) used at a dilution of 1:100. Secondary Antibody: Green-fluorescent Rabbit anti-mouse IgG-heavy and light chain cross-adsorbed Antibody DyLight 488 Conjugated (AAA213715 Lot 6) used at a dilution of 1:100 (5ug/ml). Counterstain: DAPI (blue))
IF (Immunofluorescence) (Immunofluorescence in Drosophila larvaenmJ muscle 6/7 expressing GluRIIA-GFP in neurons (GluRIIA is a post-synaptic protein) using 1st Ab anti-GFP at 1/1,000 and 2nd Ab anti-goat IgY conjugated to DyLight550 at 1/500;)
Application Data (Anti-GAPDH Ab at 1/2,500 dilution using HEK293 transfected cell lysates at 50 ug per lane; chicken polyclonal to goat IgG conjugated to DyLight 550 (AB200550) at 1/10,000 dilution;)
Goat anti Chicken IgM (Fc specific), conjugated with FITC
Reactivity
This immunoconJugate is not species-specific since Inter-species cross-reactivity is a normal feature of antisera to immunoglobulins. Cross-reactivity of this antiserum has not been tested in detail.
Hyperimmune antisera with strong precipitating activity are selected for fractionation and purification of the IgG (7S) fraction containing the bulk of the defined antibody specificity. It IS free of other serum proteins as tested by immunoelectrophoresis
Application Data (This table displays additional reactivity among various species of serum and IgA (+) indicates antibody reactivity to the corresponding target.)
WB (Western Blot) (Western Blot of Peroxidase conjugated Monkey IgG gamma antibody. Lane 1: Monkey IgG. Lane 2: none. Load: 50 ng per lane. none. Peroxidase Goat secondary antibody at 1:1,000 for 30 min at RT. Block: Blocking buffer for 30 min at RT. Size: 55 kDa for Monkey IgG Gamma..)
Goat anti Monkey IgG (HRP) was purified by delipidation, salt fractionation and ion exchange chromatography.
Pricing
ELISA (Lane 1: Rabbit IgGLane 2: Rabbit IgG Light ChainsLane 3: Rabbit IgG Heavy ChainsRabbit immunoglobulins above were resolved by electrophoresis under reducing conditions, transfered to PVDF membrane , and probed with Mouse Anti-Rabbit IgG HRP . Proteins were visulized using chemiluminescent detection.)
Application Data (ELISA plate was coated with purified goat IgG Fc and IgG Fab. Immunoglobulins were detected with serially diluted Rabbit Anti-Goat IgG Fc-HRP (SB Cat. No.AAA78879).)
IF (Immunofluorescence) (Immunofluorescence using hCEC cells, 1st Ab (anti-beta-Actin at 1/250) and 2nd Ab (anti-mouse AB27405 at 1/1,000); cells were fixed with methanol;)
IF (Immunofluorescence) (Immunofluorescence using hCEC cells, 1st Ab (anti-beta-Actin at 1/250) and 2nd Ab (anti-mouse AB27633 at 1/1,000); cells were fixed with methanol;)
IF (Immunofluorescence) (Immunofluorescence -Anti-mCherry Ab (AB9770) using hCEC cells transduced with mCherry-Rab5a; cells were fixed with methanol and mCherry Ab at 1/250; 2nd Ab goatAnti-IgY (AB307633) at 1:1,000;)
DB (Dot Blot) (Dot Blot analysis using Goat anti Rabbit IgG FITC and HRP conj ugated secondary antibody used to detect nanogram - picogram levels of rabbit IgG by dot blot on nitrocellulose membrane. 4 ul each of serial 1 in 4 dilutions of rabbit IgG were dotted on nitrocellulose and allowed to dry. Membrane was blocked in 3% BSA for 10 minutes dried for later use and rewetted with blocking buffer.)
DB (Dot Blot) (Dot Blot of Rhodamine Conjugated Goat-anti-Rabbit IgG. Antigen: Rabbit IgG. Load: Lane 1 - 50ng Lane 2 - 16.67ng Lane 3 - 5.56ng Lane 4 - 1.85ng Lane 5 - 0.62ng. Primary antibody: none. Secondary antibody: Rhodamine Conjugated Goat-a-Rabbit IgG secondary antibody at 1:1,000 for 60 min at RT. Block: MB-070 for 60 min at RT.)
WB (Western Blot) (Western Blot of Rabbit IgG Rhodamine Conjugated Secondary antibody. Lane 1: Rabbit IgG. Lane 2: None. Load: 50 ng per lane. None. Rhodamine Goat secondary antibody at 1:1,000 for 60 min at RT. Block: Blocking buffer for 30 min at RT. Size: 25 & 55 kDa, 25 & 55 kDa for Rabbit IgG..)
DB (Dot Blot) (Antigen: Rabbit IgG. Load: Lane 1 - 100 ng Lane 2 - 33.3 ng Lane 3 - 11.1 ng Lane 4 - 3.70 ng Lane 5 - 1.23 ng. Goat Fab'2 anti-Rabbit IgG Antibody (FITC) at 1:1,000 for 1 HR at RT. Block for 1 HR at RT.)
WB (Western Blot) (Western blot of FITC conjugated Goat F(ab')2 Anti-Rabbit IgG. Lane 1: Rabbit IgG. Lane 2: None. Load: 50 ng per lane. None. FITC Goat secondary antibody at 1:1,000 for 60 min at RT. Blocking: Blocking buffer for 30 min at RT. Size: 25 & 55 kDa, 25 & 55 kDa for Rabbit IgG..)
The antiSerum does not cross-react with any other component of the Horse Ig system. Inter-species cross-reactivity is a normal feature of antibodies to immunoglobulins, since Ig of different species frequently share antigenic determinants.
Secondary antibodies are immunoglobulins that bind to primary antibodies, which are directly bound to the target antigen. They are conjugated with either an enzyme, fluorophore, or biotin, and they are almost always only targeting the constant region (Fc) of the primary antibody. As a result, this amplifies the signal in various assays and helps researchers detect, quantify, and visualize specific antigens in a complex biological sample.
Key Applications of Secondary Antibodies
Western blotting for protein detection and quantification.
ELISA (Enzyme-Linked Immunosorbent Assay) for antigen-antibody interaction studies and quantification.
Immunohistochemistry (IHC) and immunofluorescence imaging for tissue and cell analysis.
Flow cytometry for cell surface and intracellular marker detection.
Immunoprecipitation (IP) and chromatin immunoprecipitation (ChIP) assays.
Signal amplification in various immunoassays.
Multiplex assays using fluorophore-conjugated secondary antibodies.
Advantages of Using Secondary Antibodies
High sensitivity
Multiple secondary antibodies can bind to a single primary antibody and amplify the signal. This is especially useful for detecting antigens even if they are in low concentrations.
Increased flexibility in assay design
Secondary antibodies come pre-conjugated with labels, such as enzymes, fluorophores, biotin, and more. This provides researchers with flexibility to use in multiple applications. They also support multiplexing for the simultaneous detection of multiple targets.
Cost-effective
Since the Fc domain remains constant within the same animal class, only one type of secondary antibody is needed to bind many types of primary antibodies. This reduces the cost of labeling multiple primary antibodies.
Better signal-to-noise ratio
Secondary antibodies minimize the background noise. As a result, they provide clearer and more accurate results.
Versatility
A single species- and isotype-specific secondary antibody can be used with any compatible primary antibody. This can help streamline reagent inventory and reduce cost and preparation time.
Easier detection
Unlike primary antibodies, secondary antibodies’ main characteristic is that they will almost always be partnered with a component that can be used for detection. This can make detection and visualization easy.
Why Buy Secondary Antibodies from AAA Biotech?
Highly Validated: Most of our secondary antibodies are thoroughly tested to ensure they work reliably across different experiments.
Versatile Applications: Our secondary antibodies can be used in a wide range of research techniques, including (but not limited to) immunocytochemistry (ICC), ELISA, immunofluorescence (IF), immunohistochemistry (IHC), flow cytometry (FC), immunoprecipitation (IP), and Western blotting (WB).
Support for Rare Species: We offer secondary antibodies specifically designed for rare or less common species—something many other suppliers don’t provide.
Affordable Prices: Our secondary antibodies are available at competitive prices to support all research budgets.
Quick and Convenient Ordering: Simple online ordering process with responsive customer support.
Privacy: We respect your privacy and ensure your information is protected at every step of the ordering process, and in all other communication with our team members.
FAQ
1. Can I reuse a secondary antibody?
Not recommended for critical experiments, as reusing may compromise sensitivity and specificity.
2. What is the difference between primary and secondary antibodies?
Primary antibodies bind directly to the antigen. Secondary antibodies bind to the primary and are usually labeled for detection.
3. How long do secondary antibodies last?
When stored properly (usually at –20°C or 4°C, depending on formulation), they can last for years. Always refer to the product datasheet.
4. What happens if you use too much secondary antibody?
Excess can increase background noise, leading to a poor signal-to-noise ratio. Titrate to find the optimal concentration.
5. Can secondary antibodies be monoclonal?
Yes. While many are polyclonal, monoclonal secondary antibodies are available for consistent batch-to-batch performance.
6. How to find secondary antibodies?
Use our catalog filters to search by host species, conjugate type, target species, and application.
7. How to store secondary antibodies?
Store at recommended temperatures away from light. Avoid repeated freeze-thaw cycles.
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