CoraLite® Plus 488-conjugated TACSTD2/TROP2 Monoclonal antibody

TACSTD2/TROP2 Monoclonal Antibody for IF/ICC

Host / Isotype

Mouse / IgG2b

Reactivity

human

Applications

IF/ICC

Conjugate

CoraLite® Plus 488 Fluorescent Dye

CloneNo.

5A6B1

Cat no : CL488-68141

Print datasheet

Synonyms

TACSTD2, GA733-1, GA733 1, GA733, EGP 1



经过测试的应用

Positive IF/ICC detected inHaCaT cells
Planning an IHC experiment? We recommend our IHCeasy TACSTD2 Ready-To-Use IHC Kit. TACSTD2 primary antibody included.
For other applications, we recommend the unconjugated version of this antibody, 68141-1-Ig

推荐稀释比

ApplicationDilution
Immunofluorescence (IF)/ICCIF/ICC : 1:50-1:500
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.

产品信息

CL488-68141 targets TACSTD2/TROP2 in IF/ICC applications and shows reactivity with human samples.

Tested Applications IF/ICC Application Description
Tested Reactivity human
Immunogen TACSTD2/TROP2 fusion protein Ag25775 种属同源性预测
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Full Name tumor-associated calcium signal transducer 2
Synonyms TACSTD2, GA733-1, GA733 1, GA733, EGP 1
Calculated Molecular Weight 36 kDa
Observed Molecular Weight40-50 kDa
GenBank Accession NumberBC009409
Gene Symbol TROP2
Gene ID (NCBI) 4070
Conjugate CoraLite® Plus 488 Fluorescent Dye
Excitation/Emission Maxima Wavelengths493 nm / 522 nm
Form Liquid
Purification MethodProtein A purification
UNIPROT IDP09758
Storage Buffer PBS with 50% Glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3.
Storage ConditionsStore at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

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).

实验方案

Product Specific Protocols
IF protocol for CL Plus 488 TACSTD2/TROP2 antibody CL488-68141Download protocol
Standard Protocols
Click here to view our Standard Protocols