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120550-35-8

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120550-35-8 Usage

Description

EZ-LINK (TM) PFP-BIOTIN, 50 MG is a chemical compound that is used for the conjugation of biotin to proteins, peptides, and other amine-containing molecules. It reacts with primary amino groups (-NH2) to form stable, irreversible amide bonds, making it a useful tool in various applications.

Uses

Used in Research and Development:
EZ-LINK (TM) PFP-BIOTIN, 50 MG is used as a conjugation agent for attaching biotin to proteins, peptides, and other amine-containing molecules for various research and development purposes. This allows for the detection, quantification, and purification of these molecules in a wide range of applications, including immunoassays, enzyme-linked immunosorbent assays (ELISA), and affinity chromatography.
Used in Diagnostics:
In the diagnostics industry, EZ-LINK (TM) PFP-BIOTIN, 50 MG is used as a labeling agent for the detection and quantification of specific proteins, peptides, and other biomolecules. The stable biotin-protein conjugates formed using this compound can be easily detected using avidin or streptavidin-based assays, providing a sensitive and reliable method for diagnostic testing.
Used in Drug Development:
EZ-LINK (TM) PFP-BIOTIN, 50 MG is also used in the pharmaceutical industry for the development of targeted drug delivery systems. By conjugating biotin to specific molecules, researchers can create targeted drug conjugates that can selectively bind to biotin receptors on the surface of cancer cells or other diseased cells, improving the specificity and efficacy of the treatment.
Used in Analytical Chemistry:
In the field of analytical chemistry, EZ-LINK (TM) PFP-BIOTIN, 50 MG is used as a derivatization agent for the analysis of amine-containing compounds. The stable biotin-amine conjugates formed using this compound can be easily detected and quantified using biotin-binding proteins, providing a sensitive and reliable method for the analysis of these compounds in various samples.

Check Digit Verification of cas no

The CAS Registry Mumber 120550-35-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,5,5 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 120550-35:
(8*1)+(7*2)+(6*0)+(5*5)+(4*5)+(3*0)+(2*3)+(1*5)=78
78 % 10 = 8
So 120550-35-8 is a valid CAS Registry Number.

120550-35-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3,4,5,6-pentafluorophenyl) 5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoate

1.2 Other means of identification

Product number -
Other names Perfluorophenyl 5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:120550-35-8 SDS

120550-35-8Relevant articles and documents

Thermoresponsive dendronized copolymers for protein recognitions based on biotin–avidin interaction

Zhou, Chunhua,Abdel-Rahman, Mona A.,Li, Wen,Liu, Kun,Zhang, Afang

, p. 832 - 838 (2017)

Thermoresponsive biotinylated dendronized copolymers carrying dendritic oligoethylene glycol (OEG) pendants were prepared via free radical polymerization, and their protein recognitions based on biotin–avidin interaction investigated. Both first (PG1) and second generation (PG2) dendronized copolymers were designed to examine possible thickness effects on the interaction between biotin and avidin. Inherited from the outstanding thermoresponsive properties from OEG dendrons, these biotinylated cylindrical copolymers show characteristic thermoresponsive behavior which provides an envelope to capture avidin through switching temperatures above or below their phase transition temperatures (Tcps). Thus, the recognition of polymer-supported biotin with avidin was investigated with UV/vis spectroscopy and dynamic laser light scattering. In contrast to the case for PG1, the increased thickness for copolymer PG2 hinders partially and inhibits the recognition of biotin moieties with avidin either below or above its Tcp. This demonstrates the significant architecture effects from dendronized polymers on the biotin moieties to shift onto periphery of the collapsed aggregates, which should be a prerequisite for protein recognition. These kinds of novel thermoresponsive copolymers may pave a way for the interesting biological applications in areas such as reversible activity control of enzyme or proteins, and for controlled delivery of drugs or genes.

Synthesis and bioactivity of labelled germination stimulants for the isolation and identification of the strigolactone receptor.

Reizelman, Anat,Wigchert, Suzanne C,del-Bianco, Cinzia,Zwanenburg, Binne

, p. 950 - 959 (2003)

Strigolactones are highly potent germination stimulants for seeds of the parasitic weeds Striga and Orobanche spp. The induction of seed germination is thought to proceed via a receptor-mediated mechanism. Isolation and purification of the strigolactone receptor by affinity chromatography using immobilized avidin or streptavidin requires a biotin labelled strigolactone analogue. For this purpose biotin has been attached, directly as well as indirectly, via a hydrophilic linker to the amino function of optically active amino-GR24. Using the same amino substituted synthetic stimulant GR24, labelled stimulants have been prepared which may be suitable for the identification of the receptor by means of fluorescence correlation spectroscopy, scanning force microscopy or photoaffinity techniques. Bioassays of the labelled stimulants reveal that the germination activity on seeds of Striga hermonthica is retained. Crystal data for the diastereoisomer (+)-8 are reported.

GENETICALLY ENCODED BIOTIN AND BIOTIN-ANALOGS AND USE THEREOF

-

Paragraph 0082, (2018/12/02)

Embodiments of the present disclosure describe non-canonical amino acids characterized by the formula A—L—B, where A is an amino acid, L is a linker, and B is a biotin or a biotin-analog group. Embodiments describe translation systems comprising an orthog

Labelling reagents having a pyridine nucleus bearing a diazomethyl function, process for synthesis of such reagents and processes for detection of biological molecules

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Page/Page column 21, (2016/03/13)

A process for synthesis of a labelling reagent, a process for the labelling of a biological molecule, a labelled biological molecule obtained by the process, a process for labelling and fragmentation of a single or double strand nucleic acid, a labelled n

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