EZ-Link™ HPDP-Biotin, No-Weigh™ Format
EZ-Link™ HPDP-Biotin, No-Weigh™ Format
Thermo Scientific™

EZ-Link™ HPDP-Biotin, No-Weigh™ Format

Thermo Scientific EZ-Link HPDP-Biotin is a membrane-permeable biotin labeling reagent that reacts with sulfhydryl (-SH) groups. The resulting disulfide bondRead more
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Catalog NumberQuantity
2134150 mg
A3539010 x 1 mg
Catalog number 21341
Price (CLP)
476.509
Each
Add to cart
Quantity:
50 mg
Request bulk or custom format
Price (CLP)
476.509
Each
Add to cart
Thermo Scientific EZ-Link HPDP-Biotin is a membrane-permeable biotin labeling reagent that reacts with sulfhydryl (-SH) groups. The resulting disulfide bond between the target sulfhydryl molecule and the biotin group can be cleaved by reducing agents to release the biotin group and regenerate the protein (or peptide) in its original, unmodified form. Labeling with HPDP-Biotin is convenient when using immobilized avidin, streptavidin, or Thermo Scientific NeutrAvidin Protein to purify the target molecules for reducing SDS PAGE or mass analysis; the captured biotinylated molecules can be efficiently eluted from the support by cleaving the disulfide bond with dithiothreitol (DTT) or other reducing agent rather than by attempting to dissociate the high affinity interaction between avidin and biotin with strong acid or denaturant.

Thermo Scientific No-Weigh products are specialty reagents provided in a pre-aliquoted format. The pre-weighed packaging prevents the loss of reagent reactivity and contamination over time by eliminating the repetitive opening and closing of the vial. The format enables use of a fresh vial of reagent each time, eliminating the hassle of weighing small amounts of reagents and reducing concerns over reagent stability.

Features of EZ-Link HPDP-Biotin:

Protein labeling—biotinylate antibodies or other proteins for use in protein methods
Thiol-reactive—reacts with sulfhydryls (-SH), such as the side-chain of cysteine (C)
Pyridyldithiol-activated—perform reactions at pH 6.5 to 7.5 in buffers such as PBS
Reversible—forms disulfide bonds, which can be cleaved using DTT or other reducing agent
Solubility—must be dissolved in DMSO or DMF before further dilution in aqueous buffers
Medium length—spacer arm (total length added to target) is 29.2 angstroms

HPDP-Biotin is a pyridyldithiol-biotin compound for labeling protein cysteines and other molecules that contain sulfhydryl groups. This reagent specifically reacts with reduced thiols (-SH) in near-neutral buffers to form reversible disulfide bonds. HPDP-Biotin is useful for labeling and affinity-purification applications that require recovery of the original, unmodified molecule. For example, a protein can be biotinylated, allowed to bind its interactor, then captured to a streptavidin column and finally eluted and recovered by reduction of the disulfide bond with dithiothreitol.

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. Three types of sulfhydryl-reactive compounds are available: maleimido, iodoacetyl and pyridyldithiol. Pyridyldithiol reagents specifically react with sulfhydryl groups (-SH) in near-neutral buffers to form reversible disulfide bonds.

In proteins, sulfhydryls exist where there are cysteine (C) residues. Cystine disulfide bonds must be reduced to make sulfhydryl groups available for labeling. Hinge-region disulfide bridges of antibodies can be selectively reduced to make functional half-antibodies that can be labeled.

Applications:
• Retrieve cell surface receptors and cleave the biotin away on an immobilized avidin column
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Cell PermeabilityCell-Permeant
Label TypeBiotin & Analogs
Product LineEZ-Link
Product TypeHPDP-Biotin
Quantity50 mg
Reactive MoietyPyridyldisulfide
Chemical ReactivityThiol
Label or DyeBiotin
SolubilityDMF (Dimethylformamide), DMSO (Dimethylsulfoxide)
SpacerLong, Cleavable
Unit SizeEach
Contents & Storage
Store at 4°C.

Frequently asked questions (FAQs)

What is the advantage of using EZ-Link HPDP-Biotin over maleimide- or iodoacetyl-containing biotinylation reagents?

Both maleimide- and iodoacetyl-containing biotinylation reagents react with sulfhydryl (-SH) groups to form stable thioether bonds that are not cleavable. EZ-Link HPDP-Biotin on the other hand is a pyridyldithiol-biotin compound that reacts with -SH groups in near-neutral buffers to form reversible disulfide bonds. Because the disulfide group can be cleaved using DTT or other reducing agents, HPDP-Biotin is useful for labeling and affinity-purification applications that require recovery of the original, unmodified molecule.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

Is it possible that HPDP-biotin (Cat. No. 21341) can also react with non-reduced sulfur?

We have no evidence that HPDP-biotin (or any pyridyldithiol compound) reacts with anything other than sulfhydryl (-SH) groups. However, many sulfur-containing compounds interconvert among several different forms. For thiouracil, with the different tautomers that are possible, the =S is in equilibrium with –SH, which can then react with the HPDP.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

Citations & References (4)

Citations & References
Abstract
A variant NuRD complex containing PWWP2A/B excludes MBD2/3 to regulate transcription at active genes.
Authors:Zhang T, Wei G, Millard CJ, Fischer R, Konietzny R, Kessler BM, Schwabe JWR, Brockdorff N
Journal:Nat Commun
PubMed ID:30228260
'Transcriptional regulation by chromatin is a highly dynamic process directed through the recruitment and coordinated action of epigenetic modifiers and readers of these modifications. Using an unbiased proteomic approach to find interactors of H3K36me3, a modification enriched on active chromatin, here we identify PWWP2A and HDAC2 among the top interactors. ... More
Splicing of long non-coding RNAs primarily depends on polypyrimidine tract and 5' splice-site sequences due to weak interactions with SR proteins.
Authors:Krchnáková Z, Thakur PK, Krausová M, Bieberstein N, Haberman N, Müller-McNicoll M, Stanek D
Journal:Nucleic Acids Res
PubMed ID:30445574
'Many nascent long non-coding RNAs (lncRNAs) undergo the same maturation steps as pre-mRNAs of protein-coding genes (PCGs), but they are often poorly spliced. To identify the underlying mechanisms for this phenomenon, we searched for putative splicing inhibitory sequences using the ncRNA-a2 as a model. Genome-wide analyses of intergenic lncRNAs (lincRNAs) ... More
The Implication of Early Chromatin Changes in X Chromosome Inactivation.
Authors:Zylicz JJ, Bousard A, Žumer K, Dossin F, Mohammad E, da Rocha ST, Schwalb B, Syx L, Dingli F, Loew D, Cramer P, Heard E
Journal:Cell
PubMed ID:30595450
'During development, the precise relationships between transcription and chromatin modifications often remain unclear. We use the X chromosome inactivation (XCI) paradigm to explore the implication of chromatin changes in gene silencing. Using female mouse embryonic stem cells, we initiate XCI by inducing Xist and then monitor the temporal changes in ... More
Bioconjugation strategy for cell surface labelling with gold nanostructures designed for highly localized pH measurement.
Authors:Puppulin L, Hosogi S, Sun H, Matsuo K, Inui T, Kumamoto Y, Suzaki T, Tanaka H, Marunaka Y
Journal:Nat Commun
PubMed ID:30538244
Regulation of intracellular pH is critically important for many cellular functions. The quantification of proton extrusion in different types of cells and physiological conditions is pivotal to fully elucidate the mechanisms of pH homeostasis. Here we show the use of gold nanoparticles (AuNP) to create a high spatial resolution sensor ... More