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Biotinylated TROP2 His&Avi Tag Protein, Human
Biotinylated TROP2 His&Avi Tag Protein, Human
Origin of place Singapore
Model UA010823-25μg
Supplier ANT BIO PTE.LTD.
Price 490
Hits 0
Updated 8/25/2025
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Product Specification


SpeciesHuman
SynonymsEGP1; TACSTD2,GA733-1,M1S1,TROP2
AccessionP09758
Amino Acid SequenceHis27-Thr274, with C-terminal His+Avi tag
Expression SystemHEK293
Molecular Weight

40-53kDa (Reducing)

Purity>95% by SDS-PAGE
Endotoxin<1EU/μg
ConjugationUnconjugated
TagAvi Tag, His Tag
Physical AppearanceLyophilized Powder
Storage BufferPBS, pH7.4.
Reconstitution

Reconstitute at 0.1-1 mg/ml according to the size in ultrapure water after rapid centrifugation.

Stability & Storage· 12 months from date of receipt, lyophilized powder stored at -20 to -80℃.
· 3 months, -20 to -80℃ under sterile conditions after reconstitution.
· 1 week, 2 to 8℃ under sterile conditions after reconstitution.
· Please avoid repeated freeze-thaw cycles.
Reference

1. Anna Shvartsur1 and Benjamin Bonavida1: Trop2 and its overexpression in cancers: regulation and clinical/therapeutic implications. Genes Cancer. 2015 Mar; 6(3-4): 84–105.

Background

Trophoblast cell-surface antigen 2 (TROP2), also known as tumor-associated calcium signal transducer 2 (TACSTD2), is a transmembrane glycoprotein with high homology to the epithelial cell. TROP2 was discovered first in trophoblast cells as a surface marker. Gene TACSTD2 located on chromosome 1p32 encodes TROP2. TROP2 consists of extracellular and transmembrane domains and a cytoplasmic tail. TROP2 undergoes intramembrane proteolysis and is cleaved into a large extracellular fragment and a short intracellular fragment. TROP2 increases intracellular calcium concentration, decreases fibronectin binding and cell adhesion, and increases cell motility. TROP2 is overexpressed in several carcinomas, such as colorectal, pancreatic, gastric, oral squamous cell carcinoma, ovarian, and breast cancers, compared with the corresponding normal tissue. Because TROP2 overexpression is associated with poor survival in patients with solid tumors, TROP2 has been considered a potential target for anticancer therapy. In studies of breast and lung cancers, TROP2 inhibition exerted anticancer effects.

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