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Human Granzyme B kit HTRF®

Cisbio's Human Granzyme B kit is designed for the rapid detection of human Granzyme B in cell supernatant and whole cells.

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  • Ready-to-use Ready-to-use
  • Highly specific Highly specific
  • Faster and more convenient than ELISA Faster and more convenient than ELISA

Cisbio's Human Granzyme B kit is designed for the rapid detection of human Granzyme B in cell supernatant and whole cells.

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Overview

Granzyme B (also called Cathepsin G-like 1, Cytotoxic T-lymphocyte proteinase 2, Fragmentin-2, Granzyme-2, or Human lymphocyte protein) is found in cytotoxic lymphocytes, NK (natural killer) cells, and cytotoxic T cells. Secreted with Perforin, which creates a pore in the cell membrane, it enters the target cell's cytoplasm and triggers apoptosis through caspase activation.

This kit is designed for the rapid detection of human Granzyme B in cell supernatant and whole cells. The assay enables high throughput without any washing steps, thereby saving time compared to ELISA.

Benefits

  • LOW SAMPLE CONSUMPTION
  • NK AND CYTOTOXIC LYMPHOCYTE T CELL FUNCTIONAL STUDY

Assay principle

Human Granzyme B is a sandwich immunoassay involving two specific anti-human Granzyme B antibodies, respectively labelled with Europium Cryptate (donor) and d2 (acceptor). The intensity of the signal is proportional to the concentration of Granzyme B present in the sample.

Principal of the HTRF Granzyme B kit

Assay Protocol

The assay protocol, using a 384-well small volume white plate or a Cisbio low volume 96-well plate (20 µL final), is described on the right. 16 µL of cell supernatant, sample, or standard are dispensed directly into the plate for detection by HTRF reagents. The antibodies labelled with HTRF donor and acceptor can be pre-mixed and added in a single dispensing step to further streamline the assay procedure. The assay can be run in 96- to 384-well plates by simply resizing each addition volume proportionally.

Protocol of the HTRF Granzyme B kit

Technical specifications of the Granzyme B kit

Sample size

16 µL

Final assay volume

20 µL

Kit components

lyophilized standard, frozen detection antibodies, buffers & protocol

LOD & LOQ (in diluent)

 1.8 ng/mL & 3.7 ng/mL

Range

3.7 – 1,500 ng/mL

Time to result

 ON at RT

Granzyme B standard curve

Recombinant Granzyme B provided in the kit (standard) was serially diluted in diluent #5, following the procedure given in the kit’s package insert. The HTRF signal, expressed as a delta ratio, was plotted as a function of the Granzyme B concentrations.

HTRF human GranzymeB standard curve

Precision

intra assay (n=24)

Sample

Mean [GranzymeB] (pg/mL)

CV

1

644

14%

2

438

14%

3

23

18%


Mean CV

15%

Each of the 3 samples was measured 24 times, and % CV was calculated for each sample.

Inter assay (n=4)

Sample

[GranzymeB]
(pg/mL)

Mean
(deltaRatio)

CV

1

10

576

9%

2

54

2759

6%

3

652

18940

6%



Mean CV

7%

Each of the samples was measured in 4 different experiments, and % CV was calculated for each sample.

Detection of Granzyme B on cell supernatant (one-plate protocol)

Different cell densities (4K and 2K) of TALL-104 cells (Effector cells) were co-cultured with or without K-562 cells (Target cells) in suspension under 16µL in 384-well sv microplates. The cells were incubated for 16 hours at 37°C - 5% CO2. After co-culture, 4 µL of the HTRF Granzyme B detection reagents were added. The HTRF signal was recorded after an overnight incubation at RT.

Granzyme B detection in a one-plate -protocol

Detection of Granzyme B on cell supernatant (Two-plate protocol)

Different cell densities (50K and 25K) of TALL-104 cells (Effector cells) were plated in suspension under 50µL in 96-well plates. TALL-104 cells were co-cultured with or without K-562 cells (Target cells) for 16 hours at 37°C - 5% CO2. After co-culture, 16µL of cell supernatants were transferred into a 384-well sv white microplate and 4 µL of the HTRF Granzyme B detection reagents were added. The HTRF signal was recorded after an overnight incubation at RT.

Granzyme B detection in a two-plate -protocol

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Plate Reader Requirement

Choosing the right microplate reader ensures you’ll get an optimal readout. Discover our high performance reader, or verify if your lab equipment is going to be compatible with this detection technology.

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