Sulfo-SBED Biotin Label Transfer Reagent, No-Weigh™ Format
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Sulfo-SBED Biotin Label Transfer Reagent, No-Weigh™ Format
Thermo Scientific™

Sulfo-SBED Biotin Label Transfer Reagent, No-Weigh™ Format

The Thermo Scientific Pierce Sulfo-SBED Biotin Label Transfer Reagent is a multifunctional reagent for labeling a purified protein and thenRead more
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Catalog NumberQuantity
A3926010 x 1 mg
3303310 mg
Catalog number A39260
Price (CNY)
3,511.00
飞享价
Ends: 31-Dec-2025
5,122.00
Save 1,611.00 (31%)
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Quantity:
10 x 1 mg
Price (CNY)
3,511.00
飞享价
Ends: 31-Dec-2025
5,122.00
Save 1,611.00 (31%)
Each
Add to cart
The Thermo Scientific Pierce Sulfo-SBED Biotin Label Transfer Reagent is a multifunctional reagent for labeling a purified protein and then covalently transferring the attached biotin tag onto specific interactors of that protein.

Sulfo-SBED is the abbreviation for Sulfo-N-hydroxysuccinimidyl-2-(6-[biotinamido]-2-(p-azido benzamido)-hexanoamido) ethyl-1,3'-dithioproprionate. It is a heterobifunctional chemical crosslinker capable of covalently attaching to primary amines at one end and to nearly any protein functional group at the other end. Unlike typical crosslinkers, Sulfo-SBED also includes a biotin group and a cleavable disulfide spacer arm. Together these features allow one to sequentially crosslink interacting proteins and transfer the biotin affinity tag from one protein (i.e., a purified 'bait' protein) to another (possibly unknown 'prey' protein). Label Transfer is a powerful in vitro method for protein interaction discovery. A growing number of publications feature the use of Sulfo-SBED Biotin Label Transfer Reagent to identify previously unknown protein interaction binding partners and to more fully characterize the specific protein binding domains of other protein interactions.

Typical protocol for label transfer experiment:

• Add a few microliters of dissolved Sulfo-SBED Reagent to 0.5-1 mL of purified bait protein in PBS.
• Incubate mixture for 30-120 minutes on ice or at room temperature in the dark.
• Desalt or dialyze (in subdued light) to remove excess non-reacted Sulfo-SBED from the labeled bait protein.
• Add labeled bait protein to cell lysate or other solution containing putative target protein interactors ('prey').
• When interaction complexes have formed, expose the solution to ultraviolet light (365 nm) for several minutes.
• Analyze products by one of several methods:
Western Blotting: Cleave crosslinks in DTT, separate proteins by SDS-PAGE, and detect biotinylated bands by Western blotting with streptavidin-HRP.
Purification and Mass Spec or Sequencing: Affinity-purify biotinylated proteins or peptide fragments following trypsin digestion and perform MS or sequencing to characterize the proteins involved.

Related Products
Sulfo-SBED Biotin Label Transfer Kit - Western Blot Application

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Chemical ReactivityAmine-to-Amine
Labeling MethodChemical Labeling, Label Transfer
Label or DyeBiotin
Product TypeSulfo-SBED Biotin Label Transfer Reagent
Quantity10 x 1 mg
Reactive MoietyNHS Ester, Alkyne
Shipping ConditionQualified for Ambient or Wet Ice
SolubilityDMF (Dimethylformamide), DMSO (Dimethylsulfoxide), Methanol, Water
Label TypeBiotin and Other Haptens
Product LinePierce
Unit SizeEach
Contents & Storage
Store at 4°C.

Frequently asked questions (FAQs)

Can you provide the shelf-life for Sulfo-SBED Biotin Label Transfer Reagent?

Sulfo-SBED Biotin Label Transfer Reagent is covered under our general 1-year warranty and is guaranteed to be fully functional for 12 months from the date of shipment, if stored as recommended. Please see section 8.1 of our Terms & Conditions of Sale (https://www.thermofisher.com/content/dam/LifeTech/Documents/PDFs/Terms-and-Conditions-of-Sale.pdf) for more details.

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

How does a product with "No-Weigh" format reduce my concern over reagent stability?

The No-Weigh product format, where small amounts of reagent are pre-weighed and packaged separately, prevents the contamination and loss of reagent reactivity over time associated with repetitive opening and closing of a single vial. This format enables use of a fresh vial of reagent each time and eliminates the hassle of weighing out small amounts of reagent. Please view additional information and the video at: https://www.thermofisher.com/us/en/home/life-science/protein-biology/protein-labeling-crosslinking/no-weigh-packaging.html

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

What crosslinkers do you recommend to study protein-protein interactions that are mass spectrometry - compatible?

We offer Sufo-SBED (Cat. Nos. 33033 and A39260).

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

What are the options for crosslinking proteins to nucleic acids, and what are the differences between them?

We offer the following crosslinkers for protein to nucleic acids: formaldehyde (Cat. No. 28906), SPB (Cat. No. 23013), SDAD (Cat. No. 26169), sulfo-SDAD (Cat. No. 26175), and sulfo-SBED (Cat. No. A39260).
Formaldehyde can be used for DNA-DNA crosslinking as well as DNA-protein crosslinking. While it is good for crosslinking proteins that are in direct contact with DNA, formaldehyde cannot link proteins that may be bound in a complex with other proteins but are not in direct contact with DNA. EGS or DSG can crosslink proteins to other proteins that are in direct contact with DNA and crosslinked to DNA by formaldehyde.
SPB, Sulfo-SDAD, and Sulfo-SBED are all photoreactive crosslinkers. SPB is an NHS-ester and psoralen heterobifunctional crosslinker that conjugates primary amines on proteins to DNA via photo-activated intercalation of psoralen to pyrimidine bases. The psoralen tricyclic planar ring system intercalates into double-stranded, and to a lesser extent, single-stranded DNA and RNA. The photoreactive psoralen group provides more selective covalent binding to nucleic acids than either phenyl azide or diazerine linkers, which makes SPB the best choice. The diazerine on sulfo-SDAD and the phenyl azide on sulfo-SBED are not selective for nucleic acids and can crosslink other biomolecules in the same besides any protein-DNA interactions. Sulfo-SBED involves biotin transfer rather than actual linking.

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