1. Immunology/Inflammation Apoptosis MAPK/ERK Pathway
  2. MHC Apoptosis JNK
  3. 1D09C3

1D09C3 is a fully human anti-HLA-DR monoclonal antibody. 1D09C3 induces apoptosis and cell death involving a cascade of events, including ROS generation, JNK activation, mitochondrial membrane depolarization, and AIF release from mitochondria. 1D09C3 shows potent anti-tumor activity and increases overall survival and median survival in JVM-2 cells and GRANTA-519 cells xenograft mice models. 1D09C3 can be used for the researches of cancer, such as chronic lymphocytic leukemia (CLL)[1][2][3].

For research use only. We do not sell to patients.

1D09C3 Chemical Structure

1D09C3 Chemical Structure

CAS No. : 791073-97-7

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Description

1D09C3 is a fully human anti-HLA-DR monoclonal antibody. 1D09C3 induces apoptosis and cell death involving a cascade of events, including ROS generation, JNK activation, mitochondrial membrane depolarization, and AIF release from mitochondria. 1D09C3 shows potent anti-tumor activity and increases overall survival and median survival in JVM-2 cells and GRANTA-519 cells xenograft mice models. 1D09C3 can be used for the researches of cancer, such as chronic lymphocytic leukemia (CLL)[1][2][3].

IC50 & Target

HLA-DR β

In Vitro

1D09C3 (2.5 µg/ mL, 24 h) significantly reduces cell countings and cell survival in HLA-DR+, but not HLA-DR- cell lines[1][2].

1D09C3 (0.1-10 µg/ mL, 4-24 h) induces a potent time- and dose-dependent death of JVM-2 and GRANTA-519 cells[1].

1D09C3 (10 µg/ mL, 4-24 h) induces cell apoptosis through a caspase-independent pathway in JVM-2 and GRANTA-519 cells[1].

1D09C3 (10 µg/ mL, 5-240 min) induces mitochondrial depolarization and generation of ROS in JVM-2 and GRANTA-519 cells[1].

1D09C3 (10 µg/ mL, 0.5-4 h) induces cell death involving activation of the JNK[1].

1D09C3 (2.5 µg/ mL, 4 h) induces cell death B-CLL cell death[1][3].

1D09C3 (10 µg/ mL, 48 h) reduces cell counts by 20% for activated T cells and by 50% for resting and activated B cells[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Proliferation Assay[1]

Cell Line: HLA-DR+ cell lines JVM-2 and GRANTA-519 and the HLA-DR cell line SU-DHL-1
Concentration: 2.5 µg/ mL
Incubation Time: 24 h
Result: Reduced the absolute number of viable cells by 3-fold and 48-fold, and the survival of tumor cells by 33-fold and 25-fold for JVM-2 and GRANTA-519, respectively

Western Blot Analysis[1]

Cell Line: JVM-2 and GRANTA-519 cells
Concentration: 10 µg/mL
Incubation Time: 4, 18 and 24 h
Result: Showed no significant change of caspase-8, 9, 3 and RARP.

Western Blot Analysis[1]

Cell Line: GRANTA-519 cells
Concentration: 10 μg/mL
Incubation Time: 0.5, 1, 2 and 4 h
Result: Upregulated the levels of JNK in mitochondrial and AIF in cytosolic.
In Vivo

1D09C3 (0.01-6 mg/mouse, i.v.) significantly increases overall survival and median survival in JVM-2 cells and GRANTA-519 cells xenograft mice models [1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: JVM-2 (1 x 106)cells xenograft mice models (NOD/SCID mice, 6-8 weeks)[1]
Dosage: 0.01 mg/mouse (day 4), 0.1 mg/mouse (day 4)
Administration: Intravenous injection
Result: Resulted in a 20% overall survival with a median survival time of 64 days.
Animal Model: JVM-2 (0.25 x 106) cells xenograft mice models (NOD/SCID mice, 6-8 weeks)[1]
Dosage: 3 x 1 mg/mouse (day 4, 7, 9) and 1 mg/mouse (day 4) for treatment of early-stage disease; 6 x 1 mg/mouse at 48-hour intervars starting onday 15 for treatment of advanced-stage disease
Administration: Intravenous injection
Result: Resulted in a 100% survival at dose up to 3 mg/mouse, and a 42% overall survival with a median survival of 99 days.
Animal Model: GRANTA-519 cells and KMS-11 cells xenograft mice models (NOD/SCID mice, 6-8 weeks)[1][2][3]
Dosage: 3 x 1 mg mouse (days 1, 4, and 7) for treatment of early-stage disease and 6 x 1 mg/mouse at 48-hour intervars starting onday 7 for treatment of advanced-stage disease
Administration: Intravenous injection
Result: Resulted in a significant increase of median survival (108 days), with 27% mice being alive and disease-free at the end of the 120-day observation period
Application

ELISA, FACS, Functional assay

Conjugated

Unconjugated

Reconsititution

The product can be reconstituted/diluted with sterile PBS or saline.

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Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

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