Ramucirumab ELISA Kit (Cyramza®) Free drug

Product type:
Biosimilar ELISA
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Ramucirumab (Cyramza®) ELISA Kit

Enzyme-linked immunosorbent assay for the quantitative determination of free Ramucirumab (Cyramza®) in serum and plasma. The Assay Genie Ramucirumab ELISA has been especially developed for the quantitative analysis of free Ramucirumab in serum and plasma and is for research use only.

Ramucirumab (Cyramza®) ELISA Kit test principle

Solid phase enzyme-linked immunosorbent assay (ELISA) based on the sandwich principle. Standards and samples (serum or plasma) are incubated in the microtitre plate coated with the reactant for ramucirumab (Cyramza®). After incubation, the wells are washed. A horse radish peroxidase (HRP) conjugated probe is added and binds to ramucirumab captured by the reactant 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 ramucirumab in the sample or standard. Results of samples can be determined directly using the standard curve.

Ramucirumab (Cyramza®) ELISA Product Information

Information Description
Free drug
Required Volume (uL)
Total Time (min)
Sample Type
Serum, Plasma
Number of Assays
Detection Limit (ng/mL)
20 (ng/mL)
Spike Recovery (%)
Shelf Life (year)

Alternative Names

Anti-VEGFR2 mAb


Ramucirumab (Cyramza®) - Key Information

Ramucirumab (Cyramza®) mode of action

Ramucirumab is a human monoclonal antibody (IgG1) against vascular endothelial growth factor receptor 2 (VEGFR2), a type II trans-membrane tyrosine kinase receptor expressed on endothelial cells. By binding to VEGFR2, ramucirumab prevents binding of its ligands (VEGF-A, VEGF-C, and VEGF-D), thereby preventing VEGF-stimulated receptor phosphorylation and downstream ligand-induced proliferation, permeability, and migration of human endothelial cells. VEGFR stimulation also mediates downstream signalling required for angiogenesis and is postulated to be heavily involved in cancer progression, making it a highly likely drug target. In contrast to other agents directed against VEGFR-2, ramucirumab binds a specific epitope on the extracellular domain of VEGFR-2, thereby blocking all VEGF ligands from binding to it.

Ramucirumab (Cyramza®) uses

Ramucirumab (Cyramza®) is used to treat stomach (gastric) cancer, colorectal cancer, Hepatocellular carcinoma or non-small cell lung cancer that has metastasized to other parts of the body. Ramucirumab (Cyramza®) may be given alone or in combination with other cancer medicines.

Ramucirumab (Cyramza®) treatment

Ramucirumab is indicated for use in advanced gastric or gastro-esophageal junction adenocarcinoma as a single agent or in combination with paclitaxel after prior fluoropyrimidine- or platinum-containing chemotherapy. According to the information given by the manufacturer; Cmax: 171 µg/ml, Cmin: 49.5 µg/ml. Ramucirumab packaging includes warnings for arterial thromboembolic events, hypertension, infusion-related reactions, gastrointestinal perforation, clinical deterioration in patients with cirrhosis, and reversible posterior leukoencephalopathy syndrome.

The most common reactions observed in single-agent-treated patients at a rate of >10% and >2% higher than placebo were hypertension and diarrhea. The most common adverse reactions observed in patients treated with ramucirumab plus paclitaxel at a rate of >30% and >2% higher than placebo plus paclitaxel were fatigue, neutropenia, diarrhea, and epistaxis.

Ramucirumab (Cyramza®) 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

7 x 0.5 mL

Standards A-E
Standard A: 600 ng/mL
Standard B: 200 ng/mL
Standard C: 60 ng/mL
Standard D: 20 ng/mL
Standard E: 0 ng/mL
Ready to use. Used for the standard curve
and control. Contains ramucirumab, human
serum and stabilizer, <0,1% NaN3.

2 x 0.5 mL


Low and high levels
Ready to use. Contains human serum and
stabilizer, <0,1% NaN3.
Control concentrations are given in “Quality
control certificate”

2 x 50 mL

Assay buffer
Ready to use. Blue coloured. Contains
proteins, <0,1% NaN3.

1 x 12 mL

Horse radish peroxidase conjugated probe
Ready to use. Red coloured. Contains HRP
conjugated probe, stabilizer and preservatives

1 x 12 mL

TMB substrate solution
Ready to use. Contains 3,3′,5,5′- Tetramethylbenzidine (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.

Ramucirumab (Cyramza®) ELISA Protocols

Steps Protocol


Pipette 50µl of Assay Buffer non-exceptionally into each of the wells to be used.


Pipette 50 µL of each “Standards”, “Low level control”, “High level control” and
diluted samples into the respective wells of microtiter plate
A1: Standard A
B1: Standard B
C1: Standard C
D1: Standard D
E1: Standard E
F1: Low level control
G1: High level control
H1 and on: Samples


Cover the plate with adhesive foil. Incubate 30 min at room temperature (18- 25°C).


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.


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


Cover the plate with adhesive foil. Incubate 30 min at room temperature (18- 25°C).


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.


Pipette 100 µL of TMB Substrate Solution into each well.


Incubate 10 min (without adhesive foil) at room temperature (18-25°C) in the dark


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.


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


CYRAMZA® is a trademark owned by or licensed to Eli Lilly and Company , its subsidiaries, or affiliates.