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Creative Biolabs

NeuroMab™ Anti-TREM2 BBB Shuttle Antibody(NRZP-1022-ZP2712)

[CAT#: NRZP-1022-ZP2712]

Host Species:
Humanized
Species Reactivity:
Human; Cynomolgus Monkey
Applications:
FC; ELISA; In Vitro; Agonist; In Vivo

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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

Humanized

Applications

FC; ELISA; In Vitro; Agonist; In Vivo

Relevant Diseases

Alzheimer's Disease
Product Properties

Storage

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

Research Use Only

For research use only
Target

Target

TREM2

Official Name

TREM2

Full Name

Triggering receptor expressed on myeloid cells 2

Alternative Names

TREM2; Triggering receptor expressed on myeloid cells 2
Product Pictures
Agonist

Figure 1 shows the increased agonistic activity of Fc variant anti-TREM2 antibodies. Luciferase activity of Fc variant antibodies co-cultured with BWZ reporter cells and THP-1 cells at a ratio of 1:1 for 6 hours.

Agonist

Figure 2 shows the increased agonistic activity of Fc variant anti-TREM2 antibodies. Luciferase activity after 6 hours of incubation with the Fc variant of an anti-TREM2 antibody.

FuncS

Figure 3 shows C3b deposition induced by Fc variant anti-TREM2 antibodies. Fold change of C3b deposition on HEK expressing TREM2 cell line for AL2p Fc variants relative to human IgG1 isotype control antibody at 10 μg/mL.

FuncS

Figure 4 shows C3b deposition induced by Fc variant anti-TREM2 antibodies. Fold change in C3b deposition of AL2p affinity matured variants with the listed Fc mutations relative to their parental IgG1 Fc variants.

FuncS

Figure 5 shows the increased activity of soluble anti-TREM2 antibodies.

FuncS

Figure 6 shows the increased activity of soluble anti-TREM2 antibodies.

FuncS

Figure 7 shows sTREM2 secreted by primary human dendritic cells from donor 534 over 48 hours after incubation with anti-TREM2 or control antibody.

FuncS

Figure 8 shows that there was no change in cell number after incubation of primary human dendritic cells from donor 534 with anti-TREM2 or control antibodies.

FuncS

Figure 9 shows plasma sTREM2 as a percentage of baseline levels following a single injection of 15 mg/kg of the TREM2 antibodies AL2p-47 huIgG1, AL2p-47 huIgG1 ASPSEG, AL2p-58 huIgG1, or control huIgG1.

FuncS

Figure 10 depicts increased viability (increased cellular ATP) after stimulation of primary human macrophages.

WB

Figure 11 shows Western blot analysis of Dap12 phosphorylation in peritoneal macrophages of WT or TREM2 Bac-Tg mice treated with AL2p-58 huIgG1, AL2p-58 huIgG1 PSEG, or control huIgG1.

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