TACSTD2/TROP2 Rekombinanter Antikörper

TACSTD2/TROP2 Rekombinant Antikörper für FC

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human

Anwendung

FC

Konjugation

Unkonjugiert

CloneNo.

250382A12

Kat-Nr. : 98465-2-RR

Synonyme

TACSTD2, Cell surface glycoprotein Trop-2, EGP 1, GA733, GA733 1

---

• 

  FC experiment of MCF-7 using 98465-2-RR

  1x10^6 MCF-7 cells were surface stained with 0.25 ug Anti-Human TACSTD2/TROP2 Rabbit RecAb (98465-2-RR, Clone: 250382A12) (red) or 0.25 ug Rabbit IgG Isotype Control RecAb (98136-1-RR, Clone: 240953C9) (blue), and PE-Conjugated Goat Anti-Rabbit IgG(H+L). Cells were not fixed.

---

Geprüfte Anwendungen

• Erfolgreiche Detektion in FC: MCF-7-Zellen

Empfohlene Verdünnung

Anwendung	Verdünnung
This reagent has been tested for flow cytometric analysis. It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, check data in validation data gallery

Produktinformation

98465-2-RR bindet in FC TACSTD2/TROP2 und zeigt Reaktivität mit human

• Getestete Reaktivität: human
• Wirt / Isotyp: Kaninchen / IgG
• Klonalität: Rekombinant
• Typ: Antikörper
• Immunogen: TACSTD2/TROP2 fusion protein Eg3329
• Vollständiger Name: tumor-associated calcium signal transducer 2
• Berechnetes Molekulargewicht: 36 kDa
• GenBank-Zugangsnummer: BC009409
• Gene symbol: TROP2
• Gene ID (NCBI): 4070
• Konjugation: Unkonjugiert
• Form: Liquid
• Reinigungsmethode: Protein-A-Reinigung
• Lagerungspuffer: PBS with 0.09% sodium azide
• Lagerungsbedingungen: Store at 2 - 8°C. Stable for one year after shipment.

Hintergrundinformationen

Trophoblast cell surface antigen 2 (TROP2), also named as TACSTD2, is a transmembrane glycoprotein. TROP2 plays a role in transducing intracellular calcium signals. It is expressed in trophoblast cells, cornea and multi-stratified epithelia. TROP2 is overexpressed in most carcinomas and is involved in cancer proliferation, migration, invasion, and metastasis. Congenital mutations of TROP2 cause a rare autosomal recessive disease which may lead to blindness-the gelatinous drop-like corneal disease (PMID: 35688908).