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HARDSHELL PCR PLATE-96, BLUE/ 50

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96-well PCR plate for robotic handling and thermal cycling. Box of 50.

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6008870

281.00 USD

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Overview
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Overview

These hard-shell 96-well skirted PCR plates are specifically designed to withstand the stresses of robotic handling and thermal cycling. The two-component design provides superior stability and flatness, allowing precise positioning for automation. The low-profile (16.05 mm) wells are optimized for low-volume reactions and fast PCR.

Key features:

Reaction volumes of 5–125 µL (200 µL maximum)
Uniform wells reduce well-to-well variability in optical assays
Full skirt for robotic handling and labeling surface
Footprint and well spacing match ANSI/SBS standard dimensions
Black lettering for easy well identification
Process sampling and testing to ensure plates are free of DNase, RNase, and human DNA

Specifications

Automation Compatible	Yes
Coating Treatment	Untreated
Color	Blue
Product Brand Name	HardShell
Shipping Condition	Ambient
Sterile	No
Unit Size	Case of 50
Wells Number	96 well plate

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Application Note

High Throughput Platforms to Characterize a Bispecific Antibody Subjected to Forced Degradation

The new bispecific antibody class (bsAbs) has emerged as one of the fastest-growing next-generation antibody therapies, due to its high specificity and low toxicity. bsAbs are designed to have two specific antigen-binding sites, unlike conventional antibody formats. Rapid and accurate functional evaluation methods and stability characterization are required to ensure product quality, safety, and efficacy.

In this study, we evaluated the stability of a bispecific mouse antibody targeting CD200 and CD47 in mouse, proteins over-expressed in many cancers, under heat stress conditions:

High throughput HTRF^® with TR-FRET (Time-Resolved Fluorescence Resonance Energy Transfer) to evaluate the effect of heat stress on the binding activity of bsAbs.
High throughput LabChip^® ProteinEXact^™ to evaluate the fragmentation of monoclonal antibodies after heat stress, and analyze different forms of bsAbs from cell culture supernatants.

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