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Citations & References (107)
Invitrogen™
Fluorescein Di-β-D-Galactopyranoside (FDG)
フルオレセイン di-β-D-ガラクトピラノシド（FDG）は、ガラクトシダーゼの最も高感度な基質の一つです。非蛍光 FDG は、β-ガラクトシダーゼによって連続的に加水分解され、最初にフルオレセインモノガラクトシド詳細を見る
| 製品番号（カタログ番号） | 数量 |
|---|---|
| F1179 | 5 mg |
製品番号（カタログ番号） F1179
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Ends: 27-Mar-2026
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Each
数量:
5 mg
フルオレセイン di-β-D-ガラクトピラノシド（FDG）は、ガラクトシダーゼの最も高感度な基質の一つです。非蛍光 FDG は、β-ガラクトシダーゼによって連続的に加水分解され、最初にフルオレセインモノガラクトシド（FMG）、次に高蛍光フルオレセインになります。酵素を介した FDG の加水分解に続いて、吸光度または蛍光のいずれかが増加する可能性があります。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
細胞透過性細胞透過性
励起／発光490⁄514
使用対象 (装置)蛍光顕微鏡、蛍光光度計、フローサイトメーター
数量5 mg
出荷条件室温
基質β-Gal基質
検出法蛍光
Substrate Properties化学基質
Unit SizeEach
組成および保存条件
冷凍庫（-5～-30℃）に保存。
引用および参考文献 (107)
引用および参考文献
Abstract
Detection of rare antigen-presenting cells by the lacZ T-cell activation assay suggests an expression cloning strategy for T-cell antigens.
Journal:Proc Natl Acad Sci U S A
PubMed ID:1378619
'The alpha/beta T-cell receptor a complex ligand formed by the association of antigenic peptides with molecules of the major histocompatibility complex (MHC). The inherent limitations of the conventional T-cell activation assays used to detect these peptide/MHC ligands have, until now, hampered the development of expression cloning systems for T-cell antigens.
Primitive adult hematopoietic stem cells can function as osteoblast precursors.
Journal:Proc Natl Acad Sci U S A
PubMed ID:14673088
'Osteoblasts are continually recruited from stem cell pools to maintain bone. Although their immediate precursor is a plastic-adherent mesenchymal stem cell able to generate tissues other than bone, increasing evidence suggests the existence of a more primitive cell that can differentiate to both hematopoietic and mesenchymal cells. We show here
Retroviral gene transfer is inhibited by chondroitin sulfate proteoglycans/glycosaminoglycans in malignant pleural effusions.
Journal:J Biol Chem
PubMed ID:9115227
'Gene therapy may be an important adjuvant for treating cancer in the pleural space. The initial results of retroviral gene transfer to cancer cells in malignant pleural effusions revealed that transduction was markedly inhibited, and studies to characterize the inhibitory factor(s) were performed. The inhibition was contained within the soluble,
In situ detection of transcriptionally active chromatin and genetic regulatory elements in individual viable mammalian cells.
Journal:Immunol Suppl
PubMed ID:2807403
'Using a newly developed FACS method for quantifying the expression of the Escherischia coli lacZ reporter gene in viable mammalian cells, we have obtained cloned cell lines in which the expression of lacZ is under the control of native endogenous transcription elements. We infected the murine pre-B cell 70Z/3 with
Transcriptional activity of the neuron-specific enolase (NSE) promoter in murine embryonic stem (ES) cells and preimplantation embryos.
Journal:Eur J Cell Biol
PubMed ID:7925488
'Mouse embryonic stem (ES) cells were transfected with a plasmid composed of an E. coli lacZ gene fused to 1.8 kb of rat neuron-specific enolase (NSE) promoter sequences. While this reporter construct had been shown previously to function exclusively in postmitotic neurons and neuro-endocrine cells of transgenic mice, stably transfected