Anti-Human IgG Fc Donor Beads
SKU: 62184685337

Anti-Human IgG Fc Donor Beads

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Description

Anti-Human IgG Fc Donor BeadsProduct Specification Stability & Storage Store in a dark place at 2 8; the product has a shelf life of 12 months. Background Homogeneous Immuno Chemiluminescence Assay (HICA) is a homogeneous immunoassay method based on energy transfer and luminescence between donor beads and acceptor beads at close proximity. Donor beads recognize protein 1 (Tag1 label), while acceptor beads recognize protein 2 (Tag2 label). When protein 1 binds to protein 2, the

Product Specification


Stability & Storage

Store in a dark place at 2-8℃; the product has a shelf life of 12 months.

Background

Homogeneous Immuno Chemiluminescence Assay (HICA) is a homogeneous immunoassay method based on energy transfer and luminescence between donor beads and acceptor beads at close proximity.

Donor beads recognize protein 1 (Tag1 label), while acceptor beads recognize protein 2 (Tag2 label). When protein 1 binds to protein 2, the distance between the beads becomes less than 200nm. Upon excitation at 680nm, the donor beads generate singlet oxygen, which diffuses to the acceptor beads. The acceptor beads then undergo a redox reaction, emitting light at 615nm. The signal intensity is directly proportional to the strength of protein interaction.

This product features a simple operation process, no washing steps, fast speed, and high sensitivity, making it suitable for detecting weak interactions.

Components

Specification

Quantity

250 μg

50 μL

5 mg

1 mL

25 mg

1 mL x 5


Protocol

[Required Reagents]

Name

Catalog No.

Anti-Human IgG Fc Donor Beads

UA086110

Streptavidin Acceptor Beads

UA086090

Universal Buffer 1

UA086113


[Reference Detection Protocol]

Procedure

Protocol 1 (37℃ Rapid Assay)

Protocol 2 (Room Temperature Assay)

Step 1:

4μL hFC tag-M1 +4μL Biotin-M2+ 6μL Anti-Human IgG Fc Donor Beads,Protect from light/Green light

4μL hFC tag-M1 +4μL Biotin-M2+ 6μL Anti-Human IgG Fc Donor Beads,Protect from light/Green light

Incubation

​37℃ shaking incubation for 20 minutes,Protect from light/Green light

​Room temperature incubation for 60 minutes,,Protect from light/Green light

Step 2:

Add 6μL Streptavidin Acceptor Beads,Protect from light/Green light

Add 6μL Streptavidin Acceptor Beads,Protect from light/Green light

Incubation

​37℃ shaking incubation for 10 minutes,Protect from light/Green light

​Room temperature incubation for 30 minutes,Protect from light/Green light

Reading

Instrument reading

Instrument reading


[Performance Validation]

Sample Preparation:

Dilute biotinylated human IgG (Bio-hIgG) to 15 μg/mL (100 nM) using Universal Buffer 1 as the stock solution, then perform serial dilutions according to the following scheme:

ID

Final Concentration (nM)

Universal Buffer 1

Volume (μL)

High Concentration Add

Volume (μL)

C12

1.0E+01

210

90 μL Stock Solution

C11

3.0E+00

210

90 μL C12

C10

1.0E+00

180

90 μL C11

C9

3.0E-01

210

90 μL C10

C8

1.0E-01

180

90 μL C9

C7

3.0E-02

210

90 μL C8

C6

1.0E-02

180

90 μL C7

C5

3.0E-03

210

90 μL C6

C4

1.0E-03

180

90 μL C5

C3

3.0E-04

210

90 μL C4

C2

1.0E-04

180

90 μL C3

C1

0

180

/


Detection Reagent Preparation:

Name

Working Concentration

Diluent

Anti-Human IgG Fc Donor Beads

25 μg/mL

Universal Buffer 1

Streptavidin Acceptor Beads

25 μg/mL

Universal Buffer 1


Results at 37℃ Incubation:

Maximum Signal: 40063

Minimum Signal: 350

EC50= 0.083 nM

Results at Room Temperature Incubation:

Maximum Signal: 27570

Minimum Signal: 172

EC50= 0.039 nM

Guidelines


1. This experiment is light-sensitive. Perform all procedures (e.g., preparation, loading, and incubation) under green light conditions (illuminance below 100 LUX).

2. This product is compatible with multifunctional microplate readers equipped with Alpha detection modules.

3. Vortex thoroughly before use. Alternatively, briefly centrifuge (2000×g, 5–10 seconds) to ensure complete sample retrieval.

4. It is recommended to use the accompanying dilution buffer for reagent preparation and sample dilution. Additional components can be directly added to this buffer if required.

5. To ensure comparability of experimental data across batches, strictly control incubation temperature and duration.

6. Avoid bubble formation during loading.

Shipping Notes
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Exchange/Return Notes
  • We offer a 30-day return/exchange service after receiving.
  • Final sale items are not eligible for returns or exchanges.
  • To process your return/exchange, please contact us at [email protected]
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SKU: 62184685337

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