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Creative Biolabs
Product

NeuroMab™ Anti-Granulin BBB Shuttle Antibody, Clone A23

[CAT#: NRZP-1022-ZP3957]

Host Species:
Mouse
Species Reactivity:
Human
Applications:
In Vitro; In Vivo; Inhib

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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

A23

Applications

In Vitro; In Vivo; Inhib
Product Properties

Storage

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

Research Use Only

For research use only
Target

Target

Granulin

Official Name

GRN

Full Name

Granulin

Alternative Names

GRN; CLN11; GEP; GP88; PCDGF; PEPI; PGranulin; granulin precursor
Product Pictures
WB

Figure 1 shows the specificity of the GEP antibody by Western blot analysis.

IHC

Figure 2 shows the localization of GEP in human liver tissue.

(A) Expression of GEP was detected in neoplastic hepatocytes (shown as brown staining), but not in other cell types of the tumor component (40X magnification). (B) Nontumorous liver tissue adjacent to the tumor (40X magnification) shows no GEP signal in the nontumorous hepatocytes.

Figure 3 shows the serum GEP concentrations of 72 healthy donors, 38 chronic hepatitis B patients and 107 HCC patients.

FuncS

Figure 4 shows the receiver operating characteristic curve analysis of serum GEP performance (thick solid line). "Sensitivity" (fraction of true positives) is plotted against "1-Specificity" (fraction of false positives).

FuncS

Figure 5 shows that in vitro treatment with A23 leads to inhibition of cell growth in a dose-dependent manner.

FuncS

Figure 6 shows growth inhibition of Hep3B tumor xenografts in nude mice. Dose-dependent effects of twice-weekly treatment with A23 in established Hep3B tumors. Antibody A23 was injected intraperitoneally as A23-50 μg (■*■) or A23-100 μg (•), and PBS was used as a control (■). Compared with PBS control, the difference is significant at *P<0.05 and **P<0.005 levels.

FuncS

Figure 7 shows the serum profile of mice on day 31 after A23 treatment. A) A23 concentration. B) GEP concentration.

FuncS

Figure 8 shows A) Histological examination of Hep3B xenografts at 200x magnification on day 31 after A23 treatment. B) Histological examination of non-neoplastic liver at day 31 after A23 treatment at 20X magnification.

FuncS

Figure 9 is the analysis of the proliferation and apoptosis of A23 in Hep3B tumors. A) Tumor cell proliferation in xenografts was assessed by Ki-67 staining. B) Apoptosis of tumor cells was assessed by TUNEL assay.

FuncS

Figure 10 shows the effect of A23 on Hep3B xenografts.

Total xenograft lysates (20 μg) were immunoblotted with the indicated phospho-specific antibodies against phospho-p44/42 MAPK (Thr202/Tyr04) and phospho-AKT (Ser473) antibodies.

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