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Optimizing BLI Assays: Effective Strategies for Reducing Non-Specific Binding

Download our new Non-Specific Binding (NSB) Application Note

Get the Complete NSB Optimization Technical Documentation

Why Download These?
Struggling with signal artifacts in complex samples?

The NSB Application Note shows you how systematic blocking strategies deliver:
✓ 90% reduction in non-specific binding
✓ 10x higher data reliability in crude lysates
✓ Accurate kinetics for low-concentration analytes
✓ Optimized protocols for BSA, detergents, and biocytin
✓ Clearer differentiation between true binding and noise

Inside you’ll find:
– Systematic NSB identification flowchart
– Step-by-step optimization protocols
– Performance data in cell culture supernatants
– Technical troubleshooting guide

Application Note Thumbnail: Optimizing BLI Assays - Effective Strategies for Reducing Non-Specific Binding (NSB)

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AI-Engineered NovoBodyTM-Based Probe for “High Capacity, Low Drift” BLI Analysis of His-Tagged Proteins

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HIS XT Probe: Advanced His-Tag Capture for Kinetics, Quantitation, and Epitope Binning

Download our new Anti-His (HIS) XT Probes Application Note and Product Note

Get the Complete HIS XT Technical Documentation

Why Download These?
Struggling with baseline drift in His-tag assays?

The HIS XT Application Note shows you how AI-designed NovoBody™ probes deliver:
✓ 58% reduction in baseline drift
✓ 4x higher signal resolution
✓ Cleaner kinetics data for weak binders
✓ Extended probe lifetime (10+ regeneration cycles)
✓ Zero Fc interference

Inside you’ll find:
– Performance comparison data
– Application protocols (kinetics, quantitation, epitope binning)
– Customer validation results
– Technical specifications

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HIS XT Biosensors for His-tagged Protein Analysis

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​​​Selection Guide: Gator Probes for His-tagged Protein Capture

Find the best probe for your His-capture assay

When working with His-tagged proteins, not all capture strategies are equal. Crude lysate introduces non-specific binding, some proteins have less-accessible tags, and high throughput assays demand faster binding steps and sensitivity. Gator® Bio offers three His-tag biosensor capture chemistries, each built for different assay needs. Choosing the right one depends on your sample matrix, your buffer composition, the affinity you need to resolve, and the speed required for your assay.

Access the full details and recommendations by downloading the Selection Guide PDF:

Download Selection Guide


Recommendations based on sample characteristics

Sample/Assay CharacteristicsAnti-His
(PN: 160009)
Ni-NTA
(PN: 160016)
Anti-His (HIS) XT
(PN: 160050)
Crude samples or complex matrices✔✔
Buffers with reducing agents or chelators✔✔
Picomolar affinity measurements✔
Small analytes (< 15 kDa) or weak interactions✔
Analysis of Fc receptor binding✔✔
Sample-limited applications✔
Standardized, high-throughput workflows in clean buffers✔✔


Table 1: Recommended His-capture probes for common sample and assay needs

The right choice usually comes down to two questions: how clean is the sample, and how sensitive does the measurement need to be. Anti-His and Anti-His XT both tolerate certain crude lysates and buffers containing reducing agents or chelators, conditions that will strip a Ni-NTA surface, because nickel-nitrilotriacetic acid coordination depends on an intact metal-chelate bond. Ni-NTA remains a strong choice for purified samples in standardized, high-throughput workflows where buffer composition is controlled. Anti-His XT is ideal for picomolar affinity work, small analytes under 15 kDa, weak interactions, and sample-limited applications where you can’t afford to use much material.


Key probe features to consider

FeatureAnti-His
(PN: 160009)
Ni-NTA
(PN: 160016)
Anti-His (HIS) XT
(PN: 160050)
Capture SurfaceMonoclonal AntibodyNi-NTA CoordinationAI-Designed NovoBody™
ApplicationsQ / K / EPQ / K / EPQ / K / EP
Quantitation Dynamic Range0.25 – 500 µg/ml0.1 – 1000 µg/ml0.2 – 1000 µg/ml
Sample RequirementsHighModerateLow
Compatible Sample MatrixPurified proteins
E coli lysate
CHO Lysate
Expi293 Lysate
Purified proteinsPurified proteins
E coli lysate
CHO lysate
Regeneration / Reuse5-10 regenerations10+ regenerations10+ regenerations
Key StrengthsSpecific His-tag recognition; compatible with many buffersSimple, widely used capture chemistry; broad dynamic rangeHigher signal response per binding event, excellent ligand affinity, low ligand use, optimized to reduce avidity

Table 2: Feature comparison between Gator Bio Anti-His, Ni-NTA, and Anti-His (HIS) XT probes

Anti-His Probes
Anti-His captures His-tagged protein through a monoclonal antibody surface. It handles purified protein, E. coli lysate, CHO lysate, and Expi293 lysate, and supports quantitation, kinetics, and epitope binning across a dynamic range of 0.25 to 500 µg/mL. The surface regenerates 5 to 10 times using Gator Regen Buffer (Salt) (PN: 120012), and its antibody-based recognition keeps working in buffers that would disrupt a metal-chelate surface.

Ni-NTA Probes
Ni-NTA uses nickel-nitrilotriacetic acid coordination to capture His-tagged protein directly, without an antibody intermediate. It’s built for purified protein in clean buffer, with a quantitation dynamic range of 0.1 to 1000 µg/mL and 10 or more regeneration cycles using Gator Ni-NTA Regen Buffer and Ni-NTA Neutral Buffer, available together as the Ni-NTA Kit. It’s a straightforward, well-established capture chemistry for labs running standardized workflows where sample purity is already controlled upstream.

Anti-His (HIS) XT Probes
Anti-His XT captures His-tagged protein using an AI-designed NovoBody™. It requires the least sample input of the three chemistries, supports a 0.2 to 1000 µg/mL dynamic range, and regenerates 10 or more times using Gator Regen Buffer pH 2.0 (no salt). The higher signal response per binding event, higher affinity His-tag capture and reduced avidity make it the choice for kinetics characterization (in particular picomolar affinity work), small analytes, and assays where sample volume is limited. See more details on HIS XT performance in our Application Note.

Download the full selection guide here:

Download Selection Guide


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