null

Rituximab (Rituxan®, Mabthera®) ELISA Kit

SKU:
HUMB00027
Product Type:
ELISA Kit
ELISA Type:
Biosimilar ELISA
Biosimilar ELISA Type:
Free drug
Applications:
ELISA
Reactivity:
Human
Analytes:
Rituximab (Rituxan®/Mabthera®)
Research Area:
Anti-Cancer
€1,019
Frequently bought together:

Description

system_update_altDatasheet

Rituximab (Rituxan®, Mabthera®) ELISA Kit

Enzyme-linked immunosorbent assay for the quantitative determination of Rituximab (Rituxan®, Mabthera®) in serum and plasma. The Assay Genie Antibody to Rituximab (Rituxan®, Mabthera®) ELISA Kit is intended for the quantitative measurement of Rituximab (Rituxan®, Mabthera®) in serum and plasma. It is for research use only. Rituxan® is a registered trademark of Biogen Idec, Inc., Mabthera® is a registered trademark of Roche, Inc.

Rituximab (Rituxan®, Mabthera®) ELISA Kit test principle

The Assay Genie rituximab (Rituxan®, Mabthera®) solid phase enzyme-linked immunosorbent assay (ELISA) is based on rituximab-specific monoclonal antibody (mAb). Standards and diluted samples are incubated in the microtitre plate coated with mAb. After incubation, the wells are washed. Anti-human IgG Fc-specific mAb conjugated to horse radish peroxidase (HRP) is added and binds to rituximab specifically captured by the human monoclonal antibody on the surface of the wells. Following incubation, wells are washed, and the bound enzymatic activity is detected by addition of chromogen-substrate. The colour developed is proportional to the amount of rituximab in the sample or standard. Results of samples can be determined directly using the standard curve.

Rituximab (Rituxan®, Mabthera®) Product Information

Information Description
Application
Free drug
Required Volume (uL)
10
Total Time (min)
135
Sample Type
Serum, Plasma
Number of Assays
96

Detection Limit (ng/mL)

3 (ng/mL)
Spike Recovery (%)
85-115%
Shelf Life (year)
1

Alternative Names

Anti-CD20 mAb

Rituxan

Rituximab (Rituxan®, Mabthera®) - Key Information

Rituximab (Rituxan®, Mabthera®) mode of action

Rituximab is a genetically engineered chimeric murine/human monoclonal antibody directed against the CD20 antigen found on the surface of normal and malignant B lymphocytes. The antibody is a glycosylated IgG1 kappa immunoglobulin containing murine light- and heavy-chain variable region sequences (Fab domain) and human constant region sequences (Fc domain). Rituximab is composed of 1,328 amino acids and has an approximate molecular weight of 144 kD. Rituximab has a high binding affinity for the CD20 antigen of 5.2 to 11.0 nM. Rituximab binds specifically to the antigen CD20, a transmembrane molecule located on pre-B and mature B lymphocytes.

Rituximab (Rituxan®, Mabthera®) uses

Rituximab is a CD20-directed cytolytic antibody indicated for the treatment of patients with: Non-Hodgkin's Lymphoma (NHL), Chronic Lymphocytic Leukemia, Rheumatoid Arthritis (RA) in combination with methotrexate in adult patients with moderately-to severely-active RA who have inadequate response to one or more TNF antagonist therapies, Wegener's Granulomatosis (WG) and Microscopic Polyangiitis (MPA) in adult patients in combination with glucocorticoids.

Rituximab (Rituxan®, Mabthera®) treatment

The CD20 antigen is expressed on > 95% of all B-cell non-Hodgkin’s lymphomas (NHL). CD20 (human B lymphocyte-restricted dif erenti tion anti en, Bp35) is a hydrophobic transmembrane protein with a molecular weight of approximately 35 kD. This non-glycosylated phosphoprotein is found on both normal and malignant B cells, but not on haematopoietic stem cells, pro-B cells, normal plasma cells or other normal tissues. CD20 regulates (an) early step(s) in the activation process for cell cycle initiation and differentiation, and possibly functions as a calcium ion channel. CD20 does not internalise upon antibody binding and is not shed from the cell surface. This antigen does not circulate in the plasma. Thus, free antigen does not compete for rituximab binding.

The Fab domain of rituximab binds to the CD20 antigen on B-lymphocytes and the Fc domain recruits immune effector functions to mediate B-cell lysis. Possible mechanisms of cell lysis include complement-dependent cytotoxicity (CDC) and antibody-dependent cellular cytotoxicity (ADCC). The antibody also induces apoptosis in the DHL-4 human B-cell lymphoma line and in vitro studies have demonstrated that rituximab sensitises drug resistant human B-cell lymphoma lines to the cytotoxic effects of some chemotherapeutic agents. In human tissue, the expression of the CD20 antigen is highly restricted; rituximab binding to CD20 was found only on lymphoid cells in the thymus, the white pulp of the spleen and a majority of B lymphocytes in peripheral blood and lymph nodes. Little or no non-specific binding was observed.

Rituximab (Rituxan®, Mabthera®) ELISA Kit Contents

Size Kit Contents

1 x 12 x 8

Microtiter Plate

Break apart strips. Microtiter plate with 12 rows each of 8 wells coated with reactant

8 x 1 mL

Rituximab Standards A-F, High Level Control, Low Level Control

300;100; 30; 10; 3; 0 nanogram/mL
Ready to use. Used for construction of the standard curve.
Contains rituximab, human serum, stabilizer and <0.1% NaN3

1 x 50 mL

Assay Buffer
Blue coloured. Ready to use. Contains proteins and <0.1% NaN3.

1 x 12 mL

Horse radish peroxidase-Conjugated Probe.

Red coloured. Ready to use. Contains HRP-probe, stabilizer and preservatives.

1 x 12 mL

TMB Substrate Solution
Ready to use. Contains TMB

1 x 12 mL

TMB Stop Solution
Ready to use. 1N HCl

1 x 50 mL

Wash Buffer concentrate (20x)
Contains Buffer with Tween 20.

2 x 1

Adhesive Foil
For covering of Microtiter Plate during incubation.


Rituximab (Rituxan®, Mabthera®) ELISA Protocol

Steps Protocol

1

Pipette 100 µL of each ready-to use Standards, High level control, Low level control and Diluted
Samples into the respective wells of microtiter plate.
Wells
A1: Standard A
B1: Standard B
C1: Standard C
D1: Standard D
E1: Standard E
F1: Standard F
G1: High Level Control
H1: Low Level Control
A2 and on: Sample (serum/plasma)

2

Cover the plate with adhesive foil. Incubate 60 min at room temperature (18- 25°C).

3

Remove adhesive foil. Discard incubation solution. Wash plate 3 times each with 300µL of diluted. Wash Buffer. Remove excess solution by tapping the inverted plate on a paper towel.

4

Pipette 100 µL of ready-to use Peroxidase Conjugate into each well.

5

Cover the plate with adhesive foil. Incubate 60 min at room temperature (18- 25°C).

6

Remove adhesive foil. Discard incubation solution. Wash plate 3 times each with 300 µL of diluted Wash Buffer. Remove excess solution by tapping the inverted plate on a paper towel.

7

Pipette 100 µL of TMB Substrate Solution into each well.

8

Incubate 15 min (without adhesive foil) at room temperature (18-25°C) in the dark

9

Stop the substrate reaction by adding 100 µL of Stop Solution into each well. Briefly mix contents by gently shaking the plate. Colour changes from blue to yellow.

10

Measure optical density with a photometer at 450/650 nm within 30 min after pipetting of the Stop Solution.

Trademarks

Rituxan® is a registered trademark of Biogen Idec, Inc.