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Creative Biolabs

NeuroMab™ Anti-TLR4 BBB Shuttle Antibody(NRZP-1022-ZP2667)

[CAT#: NRZP-1022-ZP2667]

Host Species:
Mouse
Species Reactivity:
Human; Cynomolgus Monkey
Applications:
ELISA; Block; Inhib; 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; Cynomolgus Monkey

Clonality

Monoclonal

Host Species

Mouse

Applications

ELISA; Block; Inhib; In Vitro

Relevant Diseases

Alzheimer's Disease; Parkinson's Disease; Ischemic Stroke; Multiple Sclerosis; Neuroinflammation
Product Properties

Storage

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

Research Use Only

For research use only
Target

Target

CD284

Official Name

TLR4

Full Name

Toll-like receptor 4

Alternative Names

TLR4; Toll-like receptor 4
Product Pictures
ELISA

Fig.1 is a graph depicting the binding by monoclonal phages expressing scfv to the human TLR4/MD2 complex.

The cells were incubated with either mu18H10, HTA 125 (a commercially available anti-human TLR4 non-blocking MAb) or an antibody control at the indicated concentrations and subsequently incubated with LPS (15 ng/ml). IL-8 levels were assessed 16 hours post LPS treatment.

ELISA

Fig.2 is a graph depicting the binding by purified antibodies to the human TLR4/MD2 complex.

The cells were incubated with either mu18H10, HTA 125 (a commercially available anti-human TLR4 non-blocking MAb) or an antibody control at the indicated concentrations and subsequently incubated with LPS (15 ng/ml). IL-8 levels were assessed 16 hours post LPS treatment.

ELISA

Fig.3 is a graph depicting the binding by purified antibodies, referred to herein as “1E11, 1E11 N103D”, to the cynomolgus monkey TLR4.

The cells were incubated with either mu18H10, HTA 125 (a commercially available anti-human TLR4 non-blocking MAb) or an antibody control at the indicated concentrations and subsequently incubated with LPS (15 ng/ml). IL-8 levels were assessed 16 hours post LPS treatment.

ELISA

Fig.4 is a graph depicting the binding by purified antibodies, referred to herein “1E11, 1E11 N103D”, to the human TLR4/MD2 complex.

The cells were incubated with either mu18H10, HTA 125 (a commercially available anti-human TLR4 non-blocking MAb) or an antibody control at the indicated concentrations and subsequently incubated with LPS (15 ng/ml). IL-8 levels were assessed 16 hours post LPS treatment.

Inhib

Fig.5 is a graph depicting the inhibition of LPS-induced downstream signaling cascade of TLR4, NF-κB, by purified antibodies, referred to herein “1E11, 15C1, 1C12, 1G12”.

The cells were incubated with either mu18H10, HTA 125 (a commercially available anti-human TLR4 non-blocking MAb) or an antibody control at the indicated concentrations and subsequently incubated with LPS (15 ng/ml). IL-8 levels were assessed 16 hours post LPS treatment.

Inhib

Fig.6 is a graph depicting the binding potency of purified antibodies with CDRH1 mutations, referred to herein “15C1, 1E11.C2E1, 1E11.C2E3, 1E11.C2E4, 1E11.C2E5”, to the human TLR4/MD2 complex.

The cells were incubated with either mu18H10, HTA 125 (a commercially available anti-human TLR4 non-blocking MAb) or an antibody control at the indicated concentrations and subsequently incubated with LPS (15 ng/ml). IL-8 levels were assessed 16 hours post LPS treatment.

Inhib

Fig.7 is a series of graphs depicting the inhibition of IL-6 production induced by TLR4 activation in cynomolgus monkey whole blood assay by purified antibodies, referred to herein “15C1, 1E11C2”.

The cells were incubated with either mu18H10, HTA 125 (a commercially available anti-human TLR4 non-blocking MAb) or an antibody control at the indicated concentrations and subsequently incubated with LPS (15 ng/ml). IL-8 levels were assessed 16 hours post LPS treatment.

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