Pierce™ Sulfo-SANPAH, No-Weigh™ Format
Pierce™ Sulfo-SANPAH, No-Weigh™ Format
Thermo Scientific™

Pierce™ Sulfo-SANPAH, No-Weigh™ Format

Thermo Scientific Pierce Sulfo-SANPAH is a hetero-bifunctional crosslinker that contains an amine-reactive N-hydroxysuccinimide (NHS) ester and a photoactivatable nitrophenyl azide.Leia mais
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Número do catálogoQuantity
2258950 mg
A3539510 x 1 mg
Número do catálogo 22589
Preço (BRL)
2.919,15
Each
Adicionar ao carrinho
Quantity:
50 mg
Request bulk or custom format
Preço (BRL)
2.919,15
Each
Adicionar ao carrinho
Thermo Scientific Pierce Sulfo-SANPAH is a hetero-bifunctional crosslinker that contains an amine-reactive N-hydroxysuccinimide (NHS) ester and a photoactivatable nitrophenyl azide. NHS esters react efficiently with primary amino groups (-NH2) in pH 7–9 buffers to form stable amide bonds. The reaction results in the release of sulfo-N-hydroxy-succinimide. When exposed to UV light, nitrophenyl azides form a nitrene group that can initiate addition reactions with double bonds, insertion into C-H and N-H sites, or subsequent ring expansion to react with a nucleophile (e.g., primary amines). Sulfo-SANPAH, supplied as a sodium salt, is useful for cell-surface protein crosslinking and possesses charged groups for water solubility to a concentration of 10 mM.

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 Sulfo-SANPAH:

Reactive groups: sulfo-NHS ester and nitrophenyl azide
Reactive towards: amino groups and any nucleophile
• Non-cleavable
N-Sulfosuccinimidyl-6-(4'-azido-2'-nitrophenylamino) hexanoate
• Optimal photolysis occurs at 320-350 nm; minimizes damage to biomolecules by irradiation
• Water soluble; non-cleavable

Product References:
Crosslinker Application Guide -- search for recent literature references for this product

For Research Use Only. Not for use in diagnostic procedures.
Especificações
Cell PermeabilityNo
FormPowder
Labeling MethodChemical Labeling
Molecular Weight (g/mol)492.4
PEGylatedNo
Product LinePierce
Quantity50 mg
Reactive MoietySulfo-NHS Ester, Aryl Azide
Shipping ConditionAmbient
SolubilityWater
Spacer Arm Length18.2 Å
Water SolubleYes
Chemical ReactivityAmine-Nonselective
CleavableBy Thiols
Crosslinker TypeHeterobifunctional
FormatStandard, Single-use
Product TypeCrosslinker
SpacerMedium (10 to 30 Å)
Unit SizeEach
Conteúdo e armazenamento
Upon receipt store at -20°C protected from light and moisture.

Frequently asked questions (FAQs)

Can you provide the shelf-life for Sulfo-SANPAH?

Sulfo-SANPAH 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.

What are the reactive groups on Sulfo-SANPAH and which groups do they react with?

Sulfo-SANPAH is a heterobifunctional crosslinker that has a sulfo-NHS ester and a photoactivatable nitrophenyl azide group. The sulfo-NHS ester reacts with primary amines in pH 7-9 buffers to form stable amide bonds. When exposed to UV light, nitrophenyl azides form a nitrene group that can initiate addition reactions with double bonds, insertion into C-H and N-H sites, or subsequent ring expansion to react with a nucleophile (e.g., primary amines).

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

Citações e referências (5)

Citações e referências
Abstract
Growth cones as soft and weak force generators.
Authors:Betz T, Koch D, Lu YB, Franze K, Käs JA
Journal:Proc Natl Acad Sci U S A
PubMed ID:21813757
'Many biochemical processes in the growth cone finally target its biomechanical properties, such as stiffness and force generation, and thus permit and control growth cone movement. Despite the immense progress in our understanding of biochemical processes regulating neuronal growth, growth cone biomechanics remains poorly understood. Here, we combine different experimental ... More
Tension is required but not sufficient for focal adhesion maturation without a stress fiber template.
Authors:Oakes PW, Beckham Y, Stricker J, Gardel ML
Journal:J Cell Biol
PubMed ID:22291038
Focal adhesion composition and size are modulated in a myosin II-dependent maturation process that controls adhesion, migration, and matrix remodeling. As myosin II activity drives stress fiber assembly and enhanced tension at adhesions simultaneously, the extent to which adhesion maturation is driven by tension or altered actin architecture is unknown. ... More
Periostin modulates myofibroblast differentiation during full-thickness cutaneous wound repair.
Authors:Elliott CG, Wang J, Guo X, Xu SW, Eastwood M, Guan J, Leask A, Conway SJ, Hamilton DW
Journal:J Cell Sci
PubMed ID:22266908
The matricellular protein periostin is expressed in the skin. Although periostin has been hypothesized to contribute to dermal homeostasis and repair, this has not been directly tested. To assess the contribution of periostin to dermal healing, 6 mm full-thickness excisional wounds were created in the skin of periostin-knockout and wild-type, ... More
Alpha-actinin-4 and CLP36 protein deficiencies contribute to podocyte defects in multiple human glomerulopathies.
Authors:Liu Z, Blattner SM, Tu Y, Tisherman R, Wang JH, Rastaldi MP, Kretzler M, Wu C
Journal:J Biol Chem
PubMed ID:21680739
Genetic alterations of a-actinin-4 can cause podocyte injury through multiple mechanisms. Although a mechanism involving gain-of-a-actinin-4 function was well described and is responsible for a dominantly inherited form of human focal segmental glomerulosclerosis (FSGS), evidence supporting mechanisms involving loss-of-a-actinin-4 function in human glomerular diseases remains elusive. Here we show that ... More
Contractile forces contribute to increased glycosylphosphatidylinositol-anchored receptor CD24-facilitated cancer cell invasion.
Authors:Mierke CT, Bretz N, Altevogt P
Journal:J Biol Chem
PubMed ID:21828044
The malignancy of a tumor depends on the capability of cancer cells to metastasize. The process of metastasis involves cell invasion through connective tissue and transmigration through endothelial monolayers. The expression of the glycosylphosphatidylinositol-anchored receptor CD24 is increased in several tumor types and is consistently associated with increased metastasis formation ... More