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Merck

B7639

(+)-Biotinhydrazid

≥97% (TLC), powder

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100 MG

€ 196,00

1 G

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Über diesen Artikel

Empirische Formel (Hill-System):
C10H18N4O2S
CAS-Nummer:
Molekulargewicht:
258.34
UNSPSC Code:
12352203
NACRES:
NA.46
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
28347
Assay:
≥97% (TLC)
Form:
powder

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Unterstützung erhalten

Quality Level

assay

≥97% (TLC)

form

powder

solubility

DMSO: ≤20 mg/mL

storage temp.

2-8°C

SMILES string

[H][C@]12CS[C@@H](CCCCC(=O)NN)[C@@]1([H])NC(=O)N2

InChI

1S/C10H18N4O2S/c11-14-8(15)4-2-1-3-7-9-6(5-17-7)12-10(16)13-9/h6-7,9H,1-5,11H2,(H,14,15)(H2,12,13,16)/t6-,7-,9-/m0/s1

InChI key

KOZWHQPRAOJMBN-ZKWXMUAHSA-N

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Dieser Artikel
B1267QBD10200QBD10774
assay

≥97% (TLC)

assay

≥95% (TLC)

assay

>90%

assay

>90%

Quality Level

200

Quality Level

200

Quality Level

-

Quality Level

-

solubility

DMSO: ≤20 mg/mL

solubility

acetic acid: 20 mg/mL

solubility

-

solubility

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

−20°C

form

powder

form

powder

form

solid or viscous liquid

form

solid or viscous liquid

General description

Biotin hydrazide is a biotinylation reagent used to biotinylate glycoproteins with their sugar moieties[1]. Biotin hydrazide can be used to prepare biotin-conjugated alginate[2]. It can also be used for covalent attachment to PAAc via carbodi-imide cross linking[3].

Application

(+)-Biotin hydrazide has been used:
  • the modification of alginate
  • for the labelling of mitochondrial proteins from non-muscle tissues
  • as a component of glycoprotein staining solution
  • in periodic acid-biotin-hydrazide (PABH) assay for mucins
  • for labeling surface functional groups, biologically active molecules such as antibodies, lectins, sugars, nucleic acids or molecules with free carboxylic or keto groups.
  • for coupling to glycoproteins through the carbohydrate by hydrazone formation

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Preisangaben

Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Ajay M Shah et al.
Analytical chemistry, 84(8), 3682-3688 (2012-03-15)
Microfluidic systems for affinity-based cell isolation have emerged as a promising approach for the isolation of specific cells from complex matrices (i.e., circulating tumor cells in whole blood). However, these technologies remain limited by the lack of reliable methods for
Enhanced capture and release of circulating tumor cells using hollow glass microspheres with a nanostructured surface
Dong Z, et al.
Nanoscale, 10(35), 16795-16804 (2018)
Suppressive Effect of the o-Amylase Inhibitor Albumin from Buckwheat (Fagopyrum esculentum Moench) on Postprandial Hyperglycaemia
Impact of Bioactive Peptides on Human Health, 157-157 (2016)
E P Diamandis et al.
Clinical chemistry, 37(5), 625-636 (1991-05-01)
The biotin-(strept)avidin system has been used for many years in a variety of different applications. Here we present a general overview of the system, describe its components and advantages, and show how the system is used in various applications, with
Boris Polyak et al.
Biomacromolecules, 5(2), 389-396 (2004-03-09)
Biotin was covalently coupled with alginate in an aqueous-phase reaction by means of carbodiimide-mediated activation chemistry to provide a biotin-alginate conjugate for subsequent use in biosensor applications. The synthetic procedure was optimized with respect to pH of the reaction medium

Global Trade Item Number

SKUGTIN
B7639-100MG04061833442029
B7639-1G04061826688502

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