Sulfo-SBED Biotin Label Transfer Reagent, No-Weigh™ Format
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 thenLeia mais
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Número do catálogoQuantity
3303310 mg
A3926010 x 1 mg
Número do catálogo 33033
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10 mg
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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.
Especificações
FormatPowder
Labeling MethodChemical Labeling, Label Transfer
Product TypeCrosslinker
Quantity10 mg
Reactive MoietySulfo-NHS Ester, Aryl Azide
SolubilityWater
Product LinePierce
Unit SizeEach
Conteúdo e armazenamento
Upon receipt store at 4°C.

Frequently asked questions (FAQs)

What makes Sulfo-SBED Biotin Label Transfer Reagent useful for investigation of protein interactions?

Sulfo-SBED allows one to transfer a biotin tag from an amine-containing protein to a second protein (reacted with the phenyl azide). The amine-containing protein can be removed by reduction of the disulfide in the Sulfo-SBED spacer arm. This leaves just the second biotinylated protein for detection.

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

Should the Sulfo-SBED coupling reaction be protected from light?

During the initial coupling procedure, the solutions should be protected from light to avoid decomposition of the phenyl azide functional group.

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

Which reaction should take place first during Sulfo-SBED crosslinking?

The NHS-ester end of the crosslinker is subject to hydrolysis, therefore the amine-containing protein should be conjugated prior to the photoactivatable (aryl azide) reaction.

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

What is the appropriate wavelength for the conjugation of the photoactivatable group in Sulfo-SBED Biotin Label Transfer Reagent ?

UV light at wavelengths greater than 300 nm are appropriate for conjugation.

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

Is the Sulfo-SBED crosslinker soluble in organic solutions as well as aqueous solutions?

Yes, Sulfo-SBED is soluble in aqueous as well as organic solutions. It is most soluble in organics such as DMF and DMSO.

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

Citações e referências (3)

Citações e referências
Abstract
Retagging identifies dendritic cell-specific intercellular adhesion molecule-3 (ICAM3)-grabbing non-integrin (DC-SIGN) protein as a novel receptor for a major allergen from house dust mite.
Authors:Emara M, Royer PJ, Mahdavi J, Shakib F, Ghaemmaghami AM
Journal:J Biol Chem
PubMed ID:22205703
Dendritic cells (DCs) have been shown to play a key role in the initiation and maintenance of immune responses to microbial pathogens as well as to allergens, but the exact mechanisms of their involvement in allergic responses and Th2 cell differentiation have remained elusive. Using retagging, we identified DC-SIGN as ... More
Structural basis of molecular recognition of the Leishmania small hydrophilic endoplasmic reticulum-associated protein (SHERP) at membrane surfaces.
Authors:Moore B, Miles AJ, Guerra-Giraldez C, Simpson P, Iwata M, Wallace BA, Matthews SJ, Smith DF, Brown KA
Journal:J Biol Chem
PubMed ID:21106528
The 57-residue small hydrophilic endoplasmic reticulum-associated protein (SHERP) shows highly specific, stage-regulated expression in the non-replicative vector-transmitted stages of the kinetoplastid parasite, Leishmania major, the causative agent of human cutaneous leishmaniasis. Previous studies have demonstrated that SHERP localizes as a peripheral membrane protein on the cytosolic face of the endoplasmic ... More
The interaction between cell adhesion molecule L1, matrix metalloproteinase 14, and adenine nucleotide translocator at the plasma membrane regulates L1-mediated neurite outgrowth of murine cerebellar neurons.
Authors:Loers G, Makhina T, Bork U, Dörner A, Schachner M, Kleene R
Journal:J Neurosci
PubMed ID:22423112
We have identified the adenine nucleotide translocator (ANT) isoforms ANT1 and ANT2 that are present in the plasma membrane of mouse cerebellar neurons as novel binding partners of the cell adhesion molecule L1. The direct interaction between ANT and L1 is mediated by sites within the fibronectin type III domains ... More