EZ-Link™ Biotin-LC-Hydrazide
EZ-Link™ Biotin-LC-Hydrazide
Thermo Scientific™

EZ-Link™ Biotin-LC-Hydrazide

Thermo Scientific EZ-Link Hydrazide-LC-Biotin is a mid-length, simple, hydrazide-activated biotinylation reagent for labeling glycoproteins and other carbohydrate-containing compounds having oxidizableRead more
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Catalog NumberQuantity
2134050 mg
Catalog number 21340
Price (TWD)
11,200.00
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Ends: 31-Dec-2025
16,000.00
Save 4,800.00 (30%)
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Quantity:
50 mg
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Price (TWD)
11,200.00
Online offer
Ends: 31-Dec-2025
16,000.00
Save 4,800.00 (30%)
Each
Add to cart
Thermo Scientific EZ-Link Hydrazide-LC-Biotin is a mid-length, simple, hydrazide-activated biotinylation reagent for labeling glycoproteins and other carbohydrate-containing compounds having oxidizable sugars or aldehydes.

Features of EZ-Link Biotin-LC-Hydrazide:

Glycoprotein labeling—biotinylate glycosylated proteins at sialic acid residues for detection or purification using streptavidin probes or resins
Cell surface labeling—biotinylate and isolate cell surface glycoproteins
Aldehyde-reactive—reacts with aldehydes formed by periodate-oxidation of sugar groups
Hydrazide-activated—perform reactions at pH 4 to 6 in buffers such as sodium acetate
Irreversible—forms semi-permanent hydrazone bonds; spacer arm cannot be cleaved
Solubility—usually dissolved in DMSO before further dilution in aqueous buffers
Spacer arm length—24.7Å

This biotin hydrazide reagent enables simple and efficient biotin labeling of polyclonal antibodies and other glycoproteins. Mild oxidation of antibodies with sodium periodate produces reactive aldehydes on the carbohydrate moieties of the Fc portion that can be modified by hydrazides. This approach is advantageous for labeling antibodies because biotinylation occurs only at the sites of glycosylation, which are primarily in the Fc region of the antibody, far from the antigen binding site.

We manufacture biotin reagents to ensure the highest possible overall product integrity, consistency and performance for the intended research applications.

Biotinylation reagents differ in reactivity, length, solubility, cell permeability and cleavability. Hydrazides and alkoxyamines are two types of carbonyl-reactive groups. Hydrazides (—NH-NH2) react specifically with aldehyde groups in slightly acidic conditions to form hydrazone linkages; these can be further reduced to stable secondary amine bonds using sodium cyanoborohydride (Part No. 44892). The reaction is more efficient in the presence of aniline (Part No. 88944). Alternatively, hydrazides can be conjugated to carboxylic acids using EDC carbodiimide chemistry.

Reactive aldehyde groups can be generated in glycoproteins and other polysaccharide compounds by oxidation of constituent sugar diols using sodium periodiate (Part No. 20504). Sialic acid residues are common components of protein glycosylation and are easily converted to aldehydes with 1 mM NaIO4.

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EZ-Link™ Hydrazide-Biotin
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Cell PermeabilityCell-Permeant
Label TypeBiotin & Analogs
Product LineEZ-Link
Product TypeBiotin-LC-Hydrazide
Quantity50 mg
Reactive MoietyAmine, Hydrazide
Chemical ReactivityCarboxylic Acid, Ketone, Aldehyde
Label or DyeBiotin
SolubilityDMF (Dimethylformamide), DMSO (Dimethylsulfoxide)
SpacerMid-length
Unit SizeEach
Contents & Storage
Store at 4°C.

Citations & References (2)

Citations & References
Abstract
Rare, high-affinity anti-pathogen antibodies from human repertoires, discovered using microfluidics and molecular genomics.
Authors:Adler AS, Mizrahi RA, Spindler MJ, Adams MS, Asensio MA, Edgar RC, Leong J, Leong R, Roalfe L, White R, Goldblatt D, Johnson DS
Journal:
PubMed ID:28846502
Affinity-matured, functional anti-pathogen antibodies are present at low frequencies in natural human repertoires. These antibodies are often excellent candidates for therapeutic monoclonal antibodies. However, mining natural human antibody repertoires is a challenge. In this study, we demonstrate a new method that uses microfluidics, yeast display, and deep sequencing to identify ... More
Fibroblast-specific inhibition of TGF-ß1 signaling attenuates lung and tumor fibrosis.
Authors:Wei Y, Kim TJ, Peng DH, Duan D, Gibbons DL, Yamauchi M, Jackson JR, Le Saux CJ, Calhoun C, Peters J, Derynck R, Backes BJ, Chapman HA
Journal:J Clin Invest
PubMed ID:28872461
TGF-ß1 signaling is a critical driver of collagen accumulation and fibrotic disease but also a vital suppressor of inflammation and epithelial cell proliferation. The nature of this multifunctional cytokine has limited the development of global TGF-ß1 signaling inhibitors as therapeutic agents. We conducted phenotypic screens for small molecules that inhibit ... More