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인용 및 참조 문헌 (91)
Invitrogen™
Streptavidin, Allophycocyanin, crosslinked, conjugate
Streptavidin is a bacterially derived biotin-binding protein that reportedly exhibits less nonspecific binding than avidin. Allophycocyanin is an intensely bright자세히 알아보기
| 카탈로그 번호 | 수량 |
|---|---|
| S868 | 0.5 mL |
카탈로그 번호 S868
제품 가격(KRW)
576,000
온라인 행사
Ends: 31-Mar-2026
677,000할인액 101,000 (15%)
Each
수량:
0.5 mL
제품 가격(KRW)
576,000
온라인 행사
Ends: 31-Mar-2026
677,000할인액 101,000 (15%)
Each
Streptavidin is a bacterially derived biotin-binding protein that reportedly exhibits less nonspecific binding than avidin. Allophycocyanin is an intensely bright phycobiliprotein with a broad absorption profile that peaks at ∼650 nm, and a fluorescence emission maximum of ∼660 nm.
View a selection guide for all streptavidin RPE, APC, and tandem conjugates.
View a selection guide for all streptavidin RPE, APC, and tandem conjugates.
For Research Use Only. Not for use in diagnostic procedures.
사양
농도1 mg/mL
검출 방법Fluorescence
여기/방출650/660
유세포분석기 레이저 라인633 or 635
용도(장비)Flow Cytometry, Immunoassays, Histochemical Applications, Blot Analysis
라벨 또는 염료APC (Allophycocyanin)
제품 유형Streptavidin Conjugate (Fluorescent)
수량0.5 mL
배송 조건Wet Ice
콘주게이트APC
형태Solution
Unit SizeEach
구성 및 보관
Contains 1 vial of streptavidin APC , crosslinked, conjugate (1 mg/mL).
Store in refrigerator (2–8°C) and protect from light.
Store in refrigerator (2–8°C) and protect from light.
자주 묻는 질문(FAQ)
How should I store my allophycocyanin (APC)-conjugated antibody?
인용 및 참조 문헌 (91)
인용 및 참조 문헌
Abstract
Techniques to improve the direct ex vivo detection of low frequency antigen-specific CD8+ T cells with peptide-major histocompatibility complex class I tetramers.
Journal:Cytometry A
PubMed ID:18836993
'The ability to quantify and characterize antigen-specific CD8+ T cells irrespective of functional readouts using fluorochrome-conjugated peptide-major histocompatibility complex class I (pMHCI) tetramers in conjunction with flow cytometry has transformed our understanding of cellular immune responses over the past decade. In the case of prevalent CD8+ T cell populations that
Easily reversible desthiobiotin binding to streptavidin, avidin, and other biotin-binding proteins: uses for protein labeling, detection, and isolation.
Journal:Anal Biochem
PubMed ID:12419349
'The high-affinity binding of biotin to avidin, streptavidin, and related proteins has been exploited for decades. However, a disadvantage of the biotin/biotin-binding protein interaction is that it is essentially irreversible under physiological conditions. Desthiobiotin is a biotin analogue that binds less tightly to biotin-binding proteins and is easily displaced by
Nonradioactive methods for the assay of phosphoinositide 3-kinases and phosphoinositide phosphatases and selective detection of signaling lipids in cell and tissue extracts.
Journal:Anal Biochem
PubMed ID:12605860
'We describe a novel approach to quantitation of phosphoinositides in cell extracts and in vitro enzyme-catalyzed reactions using suitably tagged and/or labeled pleckstrin homology (PH) domains as probes. Stable complexes were formed between the biotinylated target lipid and an appropriate PH domain, and phosphoinositides present in samples were detected by
Development of a ubiquitin transfer assay for high throughput screening by fluorescence resonance energy transfer.
Journal:J Biomol Screen
PubMed ID:11080690
'An assay based on fluorescence resonance energy transfer (FRET) has been developed to screen for ubiquitination inhibitors. The assay measures the transfer of ubiquitin from Ubc4 to HECT protein Rsc 1083. Secondary reagents (streptavidin and antibody to glutathione-S-transferase [GST]), pre-labeled with fluorophores (europium chelate, Eu(3+), and allophycocyanin [APC]), are noncovalently
Cell surface markers in human embryonic stem cells.
Journal:Methods Mol Biol
PubMed ID:18453248
'The pluripotent nature of human embryonic stem cells (hESCs) is based on their potential to form every cell type in the body. Prior to use in directed differentiation strategies, these cells need to be thoroughly characterized. The large number of glycoproteins and carbohydrates that exist on the cell surface provide