Key Product Details

Species Reactivity

Validated:

Mouse

Cited:

Mouse, Transgenic Mouse

Applications

Validated:

Immunohistochemistry, Western Blot, Flow Cytometry, Immunocytochemistry, CyTOF-ready

Cited:

Immunohistochemistry, Immunohistochemistry-Paraffin, Immunohistochemistry-Frozen, Western Blot, Flow Cytometry, Immunocytochemistry, In vivo assay

Label

Unconjugated

Antibody Source

Polyclonal Goat IgG
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Product Specifications

Immunogen

Mouse myeloma cell line NS0-derived recombinant mouse TROP-2
Ser82-Thr268
Accession # Q8BGV3

Specificity

Detects mouse TROP-2 in direct ELISAs and Western blots. In direct ELISAs, less than 30% cross-reactivity with recombinant human TROP‑2 is observed.

Clonality

Polyclonal

Host

Goat

Isotype

IgG

Scientific Data Images for Mouse TROP‑2 Antibody

Detection of TROP-2 antibody in mIMCD-3 Mouse Cell Line antibody by Flow Cytometry.

Detection of TROP‑2 in mIMCD-3 Mouse Cell Line by Flow Cytometry.

mIMCD-3 mouse epithelial cell line was stained with Goat Anti-Mouse TROP-2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1122, filled histogram) or isotype control antibody (Catalog # AB-108-C, open histogram), followed by Allophycocyanin-conjugated Anti-Goat IgG Secondary Antibody (Catalog # F0108).

TROP-2 antibody in XB2 Mouse Cell Line by Immunocytochemistry (ICC).

TROP‑2 in XB2 Mouse Cell Line.

TROP-2 was detected in immersion fixed XB2 mouse teratoma keratinocyte cell line using Goat Anti-Mouse TROP-2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1122) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Goat IgG Secondary Antibody (yellow; Catalog # NL001) and counterstained with DAPI (blue). View our protocol for Fluorescent ICC Staining of Cells on Coverslips.

TROP-2 antibody in Mouse Skin by Immunohistochemistry (IHC-P).

TROP‑2 in Mouse Skin.

TROP-2 was detected in immersion fixed paraffin-embedded sections of mouse skin using Goat Anti-Mouse TROP-2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1122) at 3 µg/mL for 1 hour at room temperature followed by incubation with the Anti-Goat IgG VisUCyte™ HRP Polymer Antibody (Catalog # VC004). Tissue was stained using DAB (brown) and counterstained with hematoxylin (blue). Specific staining was localized to cell membranes in keratinocytes. View our protocol for IHC Staining with VisUCyte HRP Polymer Detection Reagents.

Detection of Mouse TROP-2 by Immunohistochemistry

Detection of Mouse TROP-2 by Immunohistochemistry

Gene expression analysis of Pten mutant prostates.(A) i) Heatmap demonstrating that control samples (C1-C5) show similar expression patterns to each other, as do mutant samples (M1-M5). ii) Genes chosen for validation are indicated in heatmap derived from the average of control and mutant samples. Red indicates genes that are upregulated in mutants (116 genes), relative to controls, and green indicates genes that are downregulated in the mutants relative to controls (91 genes). (B) Quantitative RTPCR validation of indicated androgen-dependent genes differentially expressed in mutants and controls (Clu p = 0.001, Trop2 p = 0.002, Nkx3.1 p = 0.02, and Pbsn p = 0.003). mRNA accumulation was normalized to GAPDH. (C) Differential antibody staining of CLU, TROP2, and PBSN at P10 validated microarray results. (D) Whole mount in situ hybridization of Nkx3.1 shows a decrease in expression in P10 mutant prostates. The anterior prostate (AP), dorsal lateral prostate (DL) and urethra (UR) are indicated. Red arrows indicate presence of stain in the controls and absence in the mutant. “*” denotes statistical significance. Image collected and cropped by CiteAb from the following open publication (https://dx.plos.org/10.1371/journal.pone.0129470), licensed under a CC-BY license. Not internally tested by R&D Systems.
Detection of Mouse TROP-2 by Immunohistochemistry-Paraffin

Detection of Mouse TROP-2 by Immunohistochemistry-Paraffin

Pten deletion does not lead to an accumulation of progenitor cells.Antibody staining on sections of P0 and P7 prostates with antibodies to CLU and TROP2 shows no accumulation of these proteins at earlier stages of development in controls (A, B, C, D). Increased expression of these markers is seen in the mutant (E, F, G, H) relative to controls from P7. Red arrowheads indicate buds. Image collected and cropped by CiteAb from the following open publication (https://dx.plos.org/10.1371/journal.pone.0129470), licensed under a CC-BY license. Not internally tested by R&D Systems.
Detection of Mouse TROP-2 by Immunohistochemistry

Detection of Mouse TROP-2 by Immunohistochemistry

Gene expression analysis of Pten mutant prostates.(A) i) Heatmap demonstrating that control samples (C1-C5) show similar expression patterns to each other, as do mutant samples (M1-M5). ii) Genes chosen for validation are indicated in heatmap derived from the average of control and mutant samples. Red indicates genes that are upregulated in mutants (116 genes), relative to controls, and green indicates genes that are downregulated in the mutants relative to controls (91 genes). (B) Quantitative RTPCR validation of indicated androgen-dependent genes differentially expressed in mutants and controls (Clu p = 0.001, Trop2 p = 0.002, Nkx3.1 p = 0.02, and Pbsn p = 0.003). mRNA accumulation was normalized to GAPDH. (C) Differential antibody staining of CLU, TROP2, and PBSN at P10 validated microarray results. (D) Whole mount in situ hybridization of Nkx3.1 shows a decrease in expression in P10 mutant prostates. The anterior prostate (AP), dorsal lateral prostate (DL) and urethra (UR) are indicated. Red arrows indicate presence of stain in the controls and absence in the mutant. “*” denotes statistical significance. Image collected and cropped by CiteAb from the following open publication (https://dx.plos.org/10.1371/journal.pone.0129470), licensed under a CC-BY license. Not internally tested by R&D Systems.

Applications for Mouse TROP‑2 Antibody

Application
Recommended Usage

CyTOF-ready

Ready to be labeled using established conjugation methods. No BSA or other carrier proteins that could interfere with conjugation.

Flow Cytometry

0.25 µg/106 cells
Sample: mIMCD-3 Mouse Epithelial Cell Line

Immunocytochemistry

5-15 µg/mL
Sample: Immersion fixed XB2 mouse teratoma keratinocyte cell line

Immunohistochemistry

5-15 µg/mL
Sample:

Immersion fixed paraffin-embedded sections of mouse skin

Western Blot

0.1 µg/mL
Sample: Recombinant Mouse TROP‑2

Flow Cytometry Panel Builder

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Save time and reduce costly mistakes by quickly finding compatible reagents using the Panel Builder Tool.

Advanced Features

  • Spectra Viewer - Custom analysis of spectra from multiple fluorochromes
  • Spillover Popups - Visualize the spectra of individual fluorochromes
  • Antigen Density Selector - Match fluorochrome brightness with antigen density
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Formulation, Preparation, and Storage

Purification

Antigen Affinity-purified

Reconstitution

Reconstitute at 0.2 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.


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Formulation

Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.

Shipping

Lyophilized product is shipped at ambient temperature. Liquid small pack size (-SP) is shipped with polar packs. Upon receipt, store immediately at the temperature recommended below.

Stability & Storage

Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 6 months, -20 to -70 °C under sterile conditions after reconstitution.

Calculators

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

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Background: TROP-2

TROP-2, also named tumor-associated calcium signal transducer 2 (TACSTD2), GA733 tumor associated antigen, and epithelial glycoprotein-1 (EGP-1), is a type I transmembrane protein highly expressed in carcinomas. It was originally identified as an antigen present on human gastrointestinal tumors and is the second of two members of this family.  The other family member is GA7332, also called EpCAM, TROP1, 171A, gp40 and KSA.  TROP2 can transduce an intracellular calcium signal and may play a role in tumor growth. It also has adhesive functions.

Long Name

Tumor-associated Calcium Signal Transducer 2

Alternate Names

GA733-1, gp50, T16, TACSTD2, TROP2

Entrez Gene IDs

4070 (Human); 56753 (Mouse)

Gene Symbol

TACSTD2

UniProt

Additional TROP-2 Products

Product Documents for Mouse TROP‑2 Antibody

Certificate of Analysis

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Note: Certificate of Analysis not available for kit components.

Product Specific Notices for Mouse TROP‑2 Antibody

For research use only

Citations for Mouse TROP‑2 Antibody

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Protocols

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