1. Protein Tyrosine Kinase/RTK Apoptosis
  2. VEGFR Apoptosis
  3. Anti-Mouse VEGFR-2 Antibody (DC101)

Anti-Mouse VEGFR-2 Antibody (DC101) 

Cat. No.: HY-P990106 Purity: 99.41%
Technical Support

Anti-Mouse VEGFR-2 Antibody (DC101) is a rat anti-mouse VEGFR2 monoclonal antibody. Anti-Mouse VEGFR-2 Antibody (DC101) inhibits tumor angiogenesis by blocking the binding of VEGF and VEGFR2. Anti-Mouse VEGFR-2 Antibody (DC101) promotes immune cell infiltration and induces tumor cell apoptosis. Anti-Mouse VEGFR-2 Antibody (DC101) can be used for research on various types of cancer such as melanoma, lung cancer and breast cancer .

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

Size Price Stock Quantity
1 mg In-stock
5 mg In-stock
10 mg In-stock
50 mg   Get quote  
100 mg   Get quote  

* Please select Quantity before adding items.

This product is a controlled substance and not for sale in your territory.

Customer Review

Based on 1 publication(s) in Google Scholar

Top Publications Citing Use of Products

View All VEGFR Isoform Specific Products:

  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

Anti-Mouse VEGFR-2 Antibody (DC101) is a rat anti-mouse VEGFR2 monoclonal antibody. Anti-Mouse VEGFR-2 Antibody (DC101) inhibits tumor angiogenesis by blocking the binding of VEGF and VEGFR2. Anti-Mouse VEGFR-2 Antibody (DC101) promotes immune cell infiltration and induces tumor cell apoptosis. Anti-Mouse VEGFR-2 Antibody (DC101) can be used for research on various types of cancer such as melanoma, lung cancer and breast cancer [1][2][3][4][5][6].

Isotype

Rat IgG1 kappa

Recommend Isotype Controls
IC50 & Target[1][2][3][4][5][6]

VEGFR2

 

In Vivo

Anti-Mouse VEGFR-2 Antibody (DC101) (1 mg/dose, i.p., twice weekly, for 4 weeks) significantly induces apoptosis of tumor cells and endothelial cells, and significantly inhibits angiogenesis in male athymic BALB/c nude mice bearing 253J B-V tumors[1].
Anti-Mouse VEGFR-2 Antibody (DC101) (10 mg/kg, i.p., on day 2, 5 and 8) significantly inhibits tumor growth without significant toxicity in female BALB/c mice bearing H22 tumors[2].
Anti-Mouse VEGFR-2 Antibody (DC101) (40 mg/kg, i.g., once every three days, for 4 weeks) significantly inhibits tumor growth and increases immune cell infiltration in female C57BL/6 mice bearing B16-OVA tumors[3].
Anti-Mouse VEGFR-2 Antibody (DC101) (40 mg/kg, i.p., three times every week, for 21 days) significantly inhibits wound induced tumors in transgenic mice expressing CER of HPV8[4].
Anti-Mouse VEGFR-2 Antibody (DC101) (0.8 mg/mouse, i.p., twice weekly, for 2-3 weeks) inhibits tumor growth and increases T cell infiltration in FVB mice and Neu-N mice bearing NT2.5 tumors[5].
Anti-Mouse VEGFR-2 Antibody (DC101) (100 or 400 μg, i.p., once every three days, for 21 days) significantly reduces angiogenesis and endothelial cell count in female C57BL/6 mice injected with bFGF and VEGF[6].
Anti-Mouse VEGFR-2 Antibody (DC101) (800 μg, i.p., once every three days) significantly inhibits the growth of various tumors[6].

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

Animal Model: 1×106 253J B-V cells injected male athymic BALB/c nude mice (8-12 weeks)[1]
Dosage: 1 mg/dose, combined with Paclitaxel (HY-B0015) 10 mg/kg
Administration: Intraperitoneal injection (i.p.), twice weekly for 4 weeks
Result: Significantly prolonged the survival period of mice.
Significantly reduced tumor microvascular density.
Enhanced apoptosis of tumor cells and endothelial cells.
Animal Model: 2×106 H22 cells injected female BALB/c mice (6-8 weeks, 20 g)[2]
Dosage: 10 mg/kg, combined with CA4 NPs (45 mg/kg) and anti-PD-1 (100 μg/mouse)
Administration: Intraperitoneal injection (i.p.) on day 2, 5 and 8
Result: Increased the number of CD8+ T cells within the tumor.
Significantly improved vascular perfusion.
Reduced the level of IFN-γ and TNF-α.
Had good safety in vivo.
Animal Model: 5×105 B16-OVA cells injected female C57BL/6 mice (6-8 weeks)[3]
Dosage: 40 mg/kg
Administration: Oral gavage (i.g.), once every three days for 4 weeks
Result: Significantly inhibited tumor volume.
Increased infiltration of CD3+ and CD8+ T cells.
Increased infiltration of B cells (CD19+) and dendritic cells (CD11c+).
Enhanced the expression of IFN-γ, perforin, and granzyme B in CD8+ T cells.
Reduced vascular density and increased perivascular cell coverage.
Significantly increased the density of PNAd+HEV and promoted the formation of tertiary lymphoid structures (TLS).
Upregulated PD-L1 expression in tumor cells and CD45+ immune cells, as well as PD-1 expression in CD3+ T cells.
Animal Model: Transgenic mice expressing CER of HPV8[4]
Dosage: 40 mg/kg
Administration: Intraperitoneal injection (i.p.), three times every week for 21 days
Result: Reduce Ki-67+ proliferating cells and CD31+ vascular density.
Animal Model: 5×106 NT2.5 cells injected FVB mice and Neu-N mice[5]
Dosage: 0.8 mg/mouse
Administration: Intraperitoneal injection (i.p.), twice weekly for 2-3 weeks
Result: Increased CD4+ and CD8+ T cell infiltration.
Significantly inhibited tumor volume.
Decreased angiogenesis and increased tumor cell apoptosis.
Animal Model: Female C57BL/6 injected with bFGF (500 ng) and VEGF (10 μg)[6]
Dosage: 100 or 400 μg
Administration: Intraperitoneal injection (i.p.), once every three days for 21 days
Result: Significantly reduced angiogenesis and endothelial cell count in matrigel plug model.
Animal Model: 2×106 Lewis lung cells or 1×105 B16 cells injected female C57BL/6 mice (5-6 weeks), 1×105 4T1 cells injected female BALB/c mice (5-6 weeks), 2×106 A431, SK-RC-29, BxPC-3 or GBM-18 cells injected female athymic nu/nu mice (5-6 weeks)[6]
Dosage: 800 μg
Administration: Intraperitoneal injection (i.p.), once every three days
Result: Significantly inhibited tumor growth.
Gene ID

16542  [NCBI]

Accession
Application

ELISA, FACS, Functional assay, Research in vivo

Conjugated

Unconjugated

Reconsititution

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

Molecular Weight

150 kDa

Appearance

Liquid

Color

Colorless to light yellow

SMILES

[Anti-Mouse VEGFR-2 Antibody (DC101)]

Storage

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

Biological Activity
  • Immobilized VEGFR-2/Flk-1/KDR Fc Chimera Protein, Mouse can bind Anti-Mouse VEGFR-2 Antibody (DC101). The EC50 for this effect is 177.8 ng/mL.
Purity & Documentation

Purity: 99.41%

References
  • No file chosen (Maximum size is: 1024 Kb)
  • If you have published this work, please enter the PubMed ID.
  • Your name will appear on the site.
  • Molarity Calculator

  • Dilution Calculator

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass   Concentration   Volume   Molecular Weight *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Your Recently Viewed Products:

Inquiry Online

Your information is safe with us. * Required Fields.

Product Name

 

Requested Quantity *

Applicant Name *

 

Salutation

Email Address *

 

Phone Number *

Department

 

Organization Name *

City

State

Country or Region *

     

Remarks

Bulk Inquiry

Inquiry Information

Product Name:
Anti-Mouse VEGFR-2 Antibody (DC101)
Cat. No.:
HY-P990106
Quantity:
MCE Japan Authorized Agent: