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.
IHC (Immunohiostchemistry) (Ki67 was detected in paraffin-embedded sections of human intestinal cancer tissues using rabbit anti- Ki67 Antigen Affinity purified polyclonal antibody at 1 ug/mL. Cy3 Conjugated Avidin was used for visualization at 10ug/mL.)
IHC (Immunohistochemistry) (Beta Catenin was detected in paraffin-embedded sections of human intestinal cancer tissues using rabbit anti-Beta Catenin Antigen Affinity purified polyclonal antibody at 1ug/mL. Cy3 Conjugated Avidin was used for visualization at 10ug/mL.)
Goat Anti-Human IgG, Fc Fragment Specific Antibody
Applications
Western Blot, Immunohistochemistry
Purity
Immunoaffinity chromatography
Pricing
DB (Dot Blot) (Dot Blot of Goat anti-Bovine IgG Fab2 Antibody Fluorescein Conjugated. Antigen: Bovine 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. Primary antibody: n/a. Secondary antibody: Goat anti-Bovine IgG Fab2 Antibody Fluorescein Conjugated at 1:1,000 for 1 HR at RT. Block: MB-070 for 1 HR at RT.)
The antibody was isolated from ascitic by immunoaffinity chromatography using antigens coupled to agarose beads.
Pricing
WB (Western Blot) (Western blot of Peroxidase conjugated Rabbit IgG F(c) secondary antibody. Lane 1: Rabbit IgG F(c). Lane 2: None. Load: 50 ng per lane. None. Peroxidase Goat secondary antibody at 1:1,000 for 60 min at RT. Blocking: Blocking buffer for 30 min at RT. Size: 28 kDa, 28 kDa for Rabbit IgG F(c)..)
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 IgM mu antibody. Lane 1: Monkey IgM. Lane 2: none. Load: 100 ng per lane. none. Peroxidase Goat secondary antibody at 1:1,000 for 60 min at RT. Block: Blocking buffer for 30 min at RT. Observed size: 72 kDa for Rabbit IgG..)
Based on IEP and/or ELISA, reacts with whole molecular goat IgG. Also reacts with the light chains of other goat immunoglobulins. Minimal cross-reaction to Human, Mouse and Rabbit Serum Proteins.
Applications
Western Blot, Immunohistochemistry, Immunocytochemistry
Purity
Mouse anti Goat IgG (H + L) (HRP) was purified by affinity chromatography.
Pricing
IF (Immunofluorescence) (Product: Rat Anti-Mouse k-PEAmount Used: 0.1 ug/10^6 cellsCells from BALB/c spleen were double-stained with Rat Anti-Mouse K-PE and Rat Anti-Mouse CD3e-FITC (Clone C363.29B) analyzed by flow cytometry.)
Goat anti-Human Kappa (?) Light Chain - Affinity Pure, DyLight650 Conjugate, min x w/mouse serum
Reactivity
Human. Cross Reactivity: Based on IEP, no reactivity is observed to: non-immunoglobulin human serum immunoglobulins heavy chains on all human immunoglobulins lambda light chains on all human immunoglobulins mouse serum proteins
hlgG Fc: 100%; HlgA: 0%, hlgM: 0%, hlgE: 0% Reacts with the Fc portion of the heavy chain of all subclasses of human IgG as demonstrated by ELISA. May also react with igG from other species.
Applications
Western Blot, Immunohistochemistry, Immunocytochemistry, Flow Cytometry
Assay by IEP resulted in a single precipitin arc against anti-biotin, anti-Rabbit Serum, Bovine IgG, Bovine IgG F(c), and Bovine Serum. No reaction observed against Bovine IgG F(ab).
Applications
Western Blot, Immunohistochemistry
Purity
Rabbit anti Bovine IgG (biotin) was purified by delipidation, salt fractionation and ion exchange chromatography followed by dialysis.
WB (Western Blot) (Goat Anti Rabbit IgG (HRP)secondary antibody was used at 1:40,000 to detect a rabbit primary antibody by Western Blot. p27 antibody (1:1000 RT 30 minutes) showed detection of 0.1 ug of recombinant p27 protein. Lane 1: Molecular weight markers. Lane 2: MBP-p27 fusion protein (arrow; expected MW: 73.3 kDa). Lane 3: MBP alone.)
DB (Dot Blot) (Shown here is a serial 1:1 dilution of Rabbit IgG protein (250ng starting total load) co-incubated with Goat anti Rabbit IgG (HRP) and Goat anti Rabbit (Dylight 649) 1:20,000. Blot was dried and imaged (A) on Biorad Versa Doc (30 sec, DyLight649), (B) LiCor Odyssey Reader (700 nm), (C) Rewetted incubated with Femtomax 110 reimaged using BioVersaDoc (for 60 sec), (D) Incubated with TMB substrate TMBM for 5 minutes and scanned, and (E) Rewetted for Chemiluminescence and imaged for 90 sec on the BioRad VersaDoc Imager.)
DB (Dot Blot) (Dot Blot of Mouse IgG2a Antibody Alkaline Phosphatase Conjugated. Antigen: Mouse IgG2a Load: Lane 1 - 200ng Lane 2 - 66.7ng Lane 3 - 22.2ng Lane 4 - 7.4 Lane 2.5ng Primary antibody: none Secondary antibody: Mouse IgG2a Antibody Alkaline Phosphatase Conjugated at 1:1,000 for 60 min at RT. Block: MB-070 for 60 min at RT Reaction visualized using alkaline phosphatase substrate for 30 seconds at RT.)
WB (Western Blot) (Western Blot of Mouse IgG2a antibody Alkaline Phosphatase Conjugated. Lane 1: Mouse IgG2a. Lane 2: none. Load: 50ng per lane. none. Mouse IgG2a antibody Alkaline Phosphatase Conjugated at 1:1,000 o/n at 4 deg C. Block: Blocking buffer for 30 min at RT. Reaction visualized with alkaline phosphatase substrate for 30 seconds at RT. Size: 55kDa for Mouse IgG2a.)
Application Data (Lamin B1 was detected in paraffin-embedded sections of human lung cancer tissues using rabbit anti- Lamin B1 Antigen Affinity purified polyclonal antibody at 1 ug/mL. DyLight 488 Conjugated Goat Anti-rabbit IgG secondary antibody was used to detect the primary antibody at 10 ug/mL.)
Application Data (GST3/GST was detected in paraffin-embedded sections of human intestinal cancer tissues using rabbit anti-GST3/GST Antigen Affinity purified polyclonal antibody at 1 ug/mL. DyLight-488 Conjugated Goat Anti-rabbit IgG secondary antibody was used to detect the primary antibody at 10ug/mL.)
Application Data (MCM2 was detected in paraffin-embedded sections of human intestinal cancer tissues using rabbit anti- MCM2 Antigen Affinity purified polyclonal antibody at 1 ug/mL. TRITC Conjugated Goat Anti-rabbit IgG secondary antibody was used to detect the primary antibody at 30ug/mL.)
Application Data (Cpn10 was detected in paraffin-embedded sections of human mammary cancer tissues using rabbit anti- Cpn10 Antigen Affinity purified polyclonal antibody at 1 ug/mL. TRITC Conjugated Goat Anti-rabbit IgG secondary antibody was used to detect the primary antibody at 30 ug/mL.)
The antibody was purified from antisera by immunoaffinity chromatography.
Pricing
What Are Secondary Antibodies?
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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