914460
1-Biotinyl-3,6-dioxa-8-octaneamine hydrochloride
≥95%
동의어(들):
1-Biotinyl-3,6-dioxa-8-octaneamine hydrochloride, N-(2-(2-(2-aminoethoxy)ethoxy)ethyl)-5-(2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide hydrochloride, N-{2-[2-(2- Aminoethoxy)ethoxy]ethoxy}biotinamide hydrochloride, Amine-terminated biotin linker, Biotin-DOOA HCl, Biotinylation reagent
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C16H31ClN4O4S
CAS Number:
Molecular Weight:
410.96
MDL number:
UNSPSC 코드:
12352116
NACRES:
NA.22
추천 제품
![O-(2-Aminoethyl)-O′-[2-(biotinylamino)ethyl]octaethylene glycol ≥95% (oligomer uniformity)](/deepweb/assets/sigmaaldrich/product/structures/300/798/e23e92b4-9ae0-4a8d-a37e-d57a8195a30e/640/e23e92b4-9ae0-4a8d-a37e-d57a8195a30e.png)
Quality Level
분석
≥95%
양식
powder
저장 온도
2-8°C
SMILES string
S1[C@H]([C@H]2NC(=O)N[C@H]2C1)CCCCC(=O)NCCOCCOCCN.Cl
InChI
1S/C16H30N4O4S.ClH/c17-5-7-23-9-10-24-8-6-18-14(21)4-2-1-3-13-15-12(11-25-13)19-16(22)20-15;/h12-13,15H,1-11,17H2,(H,18,21)(H2,19,20,22);1H/t12-,13-,15-;/m0./s1
InChI key
UNQYTGLJZONNBD-HZPCBCDKSA-N
애플리케이션
1-Biotinyl-3,6-dioxa-8-octaneamine hydrochloride is a versatile biotinylated linker that can be incorporated into chemical tools via its terminal amino group. Labeling materials or proteins with biotin provides a means to enrich and capture targets from biological systems.
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Automate your Biotin tagging with Synple Automated Synthesis Platform (SYNPLE-SC002)
기타 정보
Efficient Innate Immune Killing of Cancer Cells Triggered by Cell Surface Anchoring of Multivalent Antibody-Recruiting Polymers
Caged Cyclopropenes with Improved Tetrazine Ligation Kinetics
A Unified Framework for the Incorporation of Bioorthogonal Compound Exposure Probes within Biological Compartments
A Chemical Probe for Protein Crotonylation
One-Step Selective Exoenzymatic Labeling (SEEL) Strategy for the Biotinylation and Identification of Glycoproteins of Living Cells
Caged Cyclopropenes with Improved Tetrazine Ligation Kinetics
A Unified Framework for the Incorporation of Bioorthogonal Compound Exposure Probes within Biological Compartments
A Chemical Probe for Protein Crotonylation
One-Step Selective Exoenzymatic Labeling (SEEL) Strategy for the Biotinylation and Identification of Glycoproteins of Living Cells
관련 제품
제품 번호
설명
가격
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
Zhiyuan Fang et al.
Chemical communications (Cambridge, England), 49(55), 6164-6166 (2013-06-04)
A direct ELISA was established for the fast detection of semicarbazide (SEM) using a novel biotin derivative. Without a tedious extraction procedure, as low as 0.07 μg L(-1) of SEM could be detected reproducibly. This assay has better recovery and
Benjamin Spangler et al.
ACS chemical biology, 14(4), 725-734 (2019-03-26)
Compartmentalization is a crucial facet of many biological systems, and key aspects of cellular processes rely on spatial segregation within the cell. While many drug targets reside in specific intracellular compartments, the tools available for assessing compound exposure are generally
Dilini N Kekulandara et al.
Biochemistry, 57(5), 772-780 (2017-12-21)
Thioredoxin 1 (Trx1) and glutaredoxin 1 (Grx1) are two ubiquitous redox enzymes that are central for redox homeostasis but also are implicated in many other processes, including stress sensing, inflammation, and apoptosis. In addition to their enzymatic redox activity, a
Sebastian Pomplun et al.
Angewandte Chemie (International ed. in English), 58(11), 3542-3547 (2019-01-18)
We discovered N-pyrrolyl alanine derivatives as efficient reagents for the fast and selective Pictet-Spengler reaction with aldehyde-containing biomolecules. Other aldehyde-labeling methods described so far have several drawbacks, like hydrolytic instability, slow reaction kinetics or not readily available labeling reagents. Pictet-Spengler
Yali Yuan et al.
Chemical communications (Cambridge, England), 54(80), 11352-11355 (2018-09-25)
We have developed highly fluorescent, monolithic colloidal CdSe seeded CdS nanorod clusters comprising thousands of nanorods. Their use in the sandwich assay detection of a model protein yields a thousand-fold improvement in the detection limit compared to individual nanorods, making
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