Human PVRL2 ELISA Kit, Lot 21AO-226 [Cancer Immune Checkpoint Assay Kit]

The kit is designed for in vitro quantitative measurement of Human PVRL2 in Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Lysate.

Custom Human Nectin-2/CD112 ELISA Kit.

ELISA

PVRL2

Human

Colorimetric

Sandwich ELISA

Quantitative

Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Lysate

This ELISA antibody pair recognizes.

Pre-Coated 96-well Strip Microplate
Wash Buffer
Stop Solution
Assay Diluent(s)
Lyophilized Standard
Biotinylated Detection Antibody
Streptavidin-Conjugated HRP
TMB One-Step Substrate

Distilled or deionized water
Precision pipettes to deliver 2 μL to 1 μL volumes
Adjustable 1-25 μL pipettes for reagent preparation
100 μL and 1 liter graduated cylinders
Tubes to prepare standard and sample dilutions
Absorbent paper
Microplate reader capable of measuring absorbance at 450nm
Log-log graph paper or computer and software for ELISA data analysis

100 μL

Pre-coated

-20 °C

The entire kit may be stored at -20°C for up to 1 year from the date of shipment. Avoid repeated freeze-thaw cycles. The kit may be stored at 4°C for up to 6 months. For extended storage, it is recommended to store at -80°C.

6 months

The entire kit may be stored at -20°C for up to 1 year from the date of shipment. Avoid repeated freeze-thaw cycles. The kit may be stored at 4°C for up to 6 months. For extended storage, it is recommended to store at -80°C.

For Research Use only

Poliovirus Receptor Related Protein 2

prr2; AI325026; AI987993; Cd112; MPH; Pvr; Pvs; nectin-2; CD112; HVEB; PRR2; PVRR2; nectin cell adhesion molecule 2; Nectin2; NECTIN2

5819

Q92692

Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process, Cell-Cell Junction Organization

1.Prepare all reagents, samples and standards as instructed in the manual.
2.Add 100 μL of standard or sample to each well.
3.Incubate 2.5 h at RT or O/N at 4°C.
4.Add 100 μL of prepared biotin antibody to each well.
5.Incubate 1 h at RT.
6.Add 100 μL of prepared Streptavidin solution to each well.
7.Incubate 45 min at RT.
8.Add 100 μL of TMB One-Step Substrate Reagent to each well.
9.Incubate 30 min at RT.
10.Add 50 μL of Stop Solution to each well.
11.Read at 450 nm immediately.