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TROP2 / TACSTD2 Antibody ( FITC ) PDF Download

Catalog Size (Price) Quantity In Stock Operation Other Information
10428-MM01-F
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TROP2 / TACSTD2 Antibody Datasheet

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TROP2 / TACSTD2 Antibody Product Information

Immunogen :

Recombinant Human TROP2 protein (Catalog#10428-H08H)

Reagents : FITC-conjugated mouse monoclonal antibody

Clone ID :

4F4B1B3

Ig Type :

 Mouse IgG1

Concentration :

5 μl/Test, 0.2 mg/ml

Formulation : Aqueous solution containing 0.5% BSA and 0.1% sodium azide
Preparation :

This antibody was produced from a hybridoma resulting from the fusion of a mouse myeloma with B cells obtained from a mouse immunized with purified, recombinant Human TROP2 / TACSTD2 (rh TROP2 / TACSTD2; Catalog#10428-H08H; NP_002344.2; Met 1-Thr 274) and conjugated with FITC under optimum conditions, the unreacted FITC was removed.

TROP2 / TACSTD2 Antibody Usage Guide

Specificity :

Human TROP2 / TACSTD2

  No cross-reactivity in ELISA with

Human E-cad

Human CD146

Human CD171

Human BCAM

Human VCAM1

Human ICAM1

Human cell lysate (293 cell line)

Flow Cytometry :

MCF-7 cells were detached using 1X trypsin, washed, then stained with FITC Mouse anti-human TROP2.

TROP2 / TACSTD2 Flow Cytometry

Flow cytometric analysis of anti-human TROP2 on MCF-7 cells.

Flow cytometry was performed on a BD FACSCalibur flow cytometry system

Please refer to www.sinobiological.com/Flow-Cytometry-FACS-Protocols-a-750.html for technical protocols.

Western blot : This antibody can be used at 1-2 μg/mL with the appropriate secondary reagents to detect Human TROP2 in WB.
Storage : This antibody is stable for 12 months from date of receipt when stored at 2℃- 8℃. Protected from prolonged exposure to light. Do not freeze !
Sodium azide is toxic to cells and should be disposed of properly. Flush with large volumes of water during disposal.

TROP2 / TACSTD2 Antibody Related Products & Topics

TROP2 / TACSTD2 Antibody Related Areas:

Stem Cell>>Embryonic Stem Cell (ESC)>>Embryonic Stem Cell Marker>>TROP-2/TACSTD2

Immunology>>Adhesion Molecule>>Cell Adhesion Molecule (IgSF CAM)>>TROP-2/TACSTD2

Proteins:

Molecule Species Description //For Detailed Info. and Price------CLICK! Cat. No
TROP-2/TACSTD2 Human TROP2/TACSTD2/Fc Protein, Recombinant 10428-H03H
TROP-2/TACSTD2 Human TROP2/TACSTD2 Protein, Recombinant 10428-H08H
TROP-2/TACSTD2 Mouse TROP2 / TACSTD2 Protein, Recombinant 50922-M02H
TROP-2/TACSTD2 Mouse TROP2 / TACSTD2 Protein, Recombinant 50922-M08H

Antibodies:

Molecule Application Description //For Detailed Info. and Price------CLICK! Cat. No
Human
TROP-2/TACSTD2
ELISA Mouse Monoclonal Antibody 10428-MM01
Human
TROP-2/TACSTD2
WB Mouse Monoclonal Antibody 10428-MM02
Human
TROP-2/TACSTD2
WB Mouse Monoclonal Antibody 10428-MM01-F
Human
TROP-2/TACSTD2
WB, ELISA TROP2 / TACSTD2 Antibody 10428-R001
Human
TROP-2/TACSTD2
WB, ELISA TROP-2/TACSTD2 Antibody, Rabbit MAb 10428-R030
Human
TROP-2/TACSTD2
WB, ELISA Rabbit Polyclonal Antibody 10428-RP01
Human
TROP-2/TACSTD2
WB, ELISA Rabbit Polyclonal Antibody (Antigen Affinity Purified) 10428-RP02

TROP2 / TACSTD2 Antibody Background

TROP2, also referred to as tumor associated calcium signal transducer 2 (TACSTD2), GA733-1 or M1S1, is a cell surface glycoprotein highly expressed by human carcinomas. TROP2 encoding by an intronless gene was originally defined by the monoclonal antibody GA733, and is a member of a family of at least two type I membrane proteins. The other known member is GA733-2, also called EpCAM and TROP1. It has been suggested by studies that the GA733-1 gene was formed by the retroposition of the GA733-2 gene via an mRNA intermediate. The cytoplasmic tail of TROP2 possesses potential serine and tyrosine phosphorylation sites and a conserved phosphatidyl-inositol binding consensus sequence. TROP2 transduces an intracellular calcium signal and acts as a cell surface receptor, meanwhile is involved in the regulation of cell- cell adhesion. Accordingly, as a widespread stimulator of human cancer growth and a unique marker and causal factor of metastatic cancer, TROP2 is a possible candidate for diagnosis and molecular target therapy. Mutations of this gene result in gelatinous drop-like corneal dystrophy, an autosomal recessive disorder characterized by severe corneal amyloidosis leading to blindness.

References

  1. Fornaro, M. et al., 1995, Int. J. Cancer. 62: 610-618.
  2. Ripani, E. et al., 1998, Int. J. Cancer. 76: 671-676.
  3. Linnenbach, A.J. et al., 1993, Mol. Cell. Biol. 13: 1507-1515.
  4. Ohmachi, T. et al., 2006, Clin. Cancer. Res. 12: 3057-3063.
  5. Tsujikawa, M. et al., 1999, Nat. Genet. 21: 420-423.