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Creative Biolabs

NeuroMab™ Anti-FGFR1 BBB Shuttle Antibody(NRZP-1022-ZP3892)

[CAT#: NRZP-1022-ZP3892]

Host Species:
Humanized
Species Reactivity:
Human
Applications:
WB; ELISA; In Vitro; In Vivo; Agonist

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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

Humanized

Applications

WB; ELISA; In Vitro; In Vivo; Agonist

Relevant Diseases

Multiple Sclerosis; Glioma
Product Properties

Storage

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

Research Use Only

For research use only
Target

Target

FGFR1

Official Name

FGFR1

Full Name

Fibroblast Growth Factor Receptor 1

Alternative Names

Fibroblast Growth Factor Receptor 1; Basic Fibroblast Growth Factor Receptor 1; Fms-Related Tyrosine Kinase 2; Proto-Oncogene C-Fgr; EC 2.7.10.1; BFGF-R-1; FGFR-1; N-SAM; BFGFR; FGFBR; FLT-2; HBGFR; FLT2; CEK; FLG;
Product Pictures
ELISA

Figure 1 shows ELISA measurement of binding of anti-FGFR1 antibody to purified FGFR ECD fragment.

Figure 2A shows cumulative food intake, blood glucose and body weight changes in lean C57BL/6 mice following a single intraperitoneal injection of 0.5 mpk of R1MAb1 or control IgG.

Figure 2B shows a glucose tolerance test performed with an intraperitoneal injection of 2 g/kg glucose on day 4 after an overnight fast.

Figure 3 shows gene expression analysis using mRNA isolated from mouse liver tissue.

Figure 4 shows gene expression analysis using mRNA isolated from mouse brown adipose tissue.

ELISA

Figure 5A shows the results of an ELISA measuring antibody binding to biotinylated peptide fragments.

ELISA

Figure 5B shows the results of an ELISA measuring the binding of His-tagged FGFR1 to FGF2 protein in the presence of various concentrations of R1MAb1 or control IgG. Data are expressed as % FGFR1-His binding and represent mean ± SEM (n=3).

Figure 6 shows non-specific binding in the presence of various concentrations of unlabeled R1MAb1 or FGF21 (reactions also contained BSA (10 mg/ml) and control IgG (350 mM). Data are expressed as total radiolabeled FGF21 in the reaction percent of bound FGF21.

Figure 7 shows the requirement of FGF21 and R1 MAb activity for normal adipose function.

Figure 8 shows blood glucose (left) and body weight (right) of db/db mice after a single intraperitoneal injection of the indicated Abs on day 0 (arrows). N=7 *p<0.05 (control IgG vs. 3 mpk R1MAb 1), **p<0.0005 (control IgG vs. 3 mpk R1MAb1 and control IgG vs. 1 mpk R1MAb 1).

Figure 9 shows Western blot analysis of 3T3-L1 adipocytes treated with 0.5 μg/ml of the indicated proteins for the indicated times.

Figure 10 shows HFD-fed mice performed with GTT in S3B at day 8 after Ab injection. After overnight fasting, mice were intraperitoneally injected with 1 g/kg glucose. Mean body weight was 28.6+/-0.6 (R1MAb1) and 32.1+/-0.8 (control IgG) (p<0.01). N=7.

Figure 11 shows blood glucose (left) and body weight (right) of HFD-fed C57BL/6 mice following a single intraperitoneal injection of R1 Mabl or control IgG at 1 mpk on day 0. N=7~9 *p<0.05.

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