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Creative Biolabs
Product

NeuroMab™ Anti-Amyloid Beta BBB Shuttle Antibody, Clone mAb31

[CAT#: NRZP-1022-ZP4049]

Host Species:
Mouse
Species Reactivity:
Human
Applications:
In Vitro

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Product Overview

Description

Brain uptake of therapeutic antibodies is severely limited by their size. To achieve enhanced BBB crossing, Creative Biolabs developed a BBB shuttle antibody platform by utilizing the endogenous macromolecule transportation pathway, known as receptor-mediated transcytosis (RMT). The engineered antibody-based carrier is believed to significantly to increase the macromolecule brain entry to combat CNS diseases.
Notes: The BBB antibody is made-to order and available in a customized format. Please don't hesitate contact us for more details.

Species Reactivity

Human

Clonality

Monoclonal

Host Species

Mouse

Clone Number

mAb31

Applications

In Vitro
Product Properties

Storage

Store at -20°C. Do not aliquot the antibody.

Research Use Only

For research use only
Target

Target

Amyloid Beta

Official Name

Amyloid Beta

Full Name

Amyloid Beta

Alternative Names

APP; Aβ; Abeta; Amyloid β
Product Pictures
ELISA

Figure 1 Binding properties of the fusion protein to the Aβ structure.

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Figure 2 Plaque decoration of anti-Aβ monoclonal antibody mAb31.

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Figure 3 shows the quantification of the dual Fab-mAb31 construct.

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Figure 4 shows the quantification of individual Fab-mAb31 constructs.

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Figure 5 Plaque decoration of two different doses of anti-Aβ monoclonal antibody mAb31 and a very low dose of single Fab mAb31 (single Fab fused to the C-terminus of mAb31)

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Figure 6 Quantitative expression of TfR cells treated with single Fab-mab31 or double Fab-mAb31

In Vivo

Figure 7 In vivo cellular trafficking of TfR treated with single Fab-mab31 or double Fab-mAb31.

In Vivo

Figure 8 In vivo cellular trafficking of TfR treated with single Fab-mab31 or double Fab-mAb31.

ADCC

Figure 9 Antibody multimers with TfR scFab fragments fused to the Fc C-terminus do not induce ADCC.

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Figure 10 Quantitative morphological analysis of plaque immunohistochemical staining showing cortex and hippocampus.

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Figure 11 demonstrates that a low dose of the sFab construct (2.66 mg/kg) reached plaques in the brain rapidly and significantly compared to mAb31 at 2 mg/kg and 10 mg/kg.

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Figure 12 In vivo cellular trafficking of TfR treated with double Fab-mab31.

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Figure 13 In vivo cellular trafficking of TfR treated with a single Fab-mab31.

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