About This Item
Fórmula empírica (Notação de Hill):
C12H12O10N2
Número CAS:
Peso molecular:
344.23
Número MDL:
Código UNSPSC:
12352200
ID de substância PubChem:
Produtos recomendados
Ensaio
≥85%
forma
powder
peso molecular
344.24
adequação da reação
reagent type: cross-linking reagent
condição de armazenamento
desiccated
solubilidade
DMSO or DMF: soluble
Condições de expedição
ambient
temperatura de armazenamento
2-8°C
cadeia de caracteres SMILES
O=C(C(O)C(O)C(ON1C(CCC1=O)=O)=O)ON2C(CCC2=O)=O
InChI
1S/C12H12N2O10/c15-5-1-2-6(16)13(5)23-11(21)9(19)10(20)12(22)24-14-7(17)3-4-8(14)18/h9-10,19-20H,1-4H2
chave InChI
NXVYSVARUKNFNF-UHFFFAOYSA-N
Descrição geral
DST is a homobifunctional crosslinker that contains amine-reactive N-hydroxysuccinimide (NHS) ester groups and is periodate cleavable. DST is commonly used for conjugating radiolabeled ligands to cell surface receptors. DST must first be dissolved in an organic solvent, such as DMSO or DMF, then added to the aqueous reaction mixture. DST is lipophilic, membrane-permeable and does not possess a charged group, which makes it useful for intracellular and intramembrane protein conjugation.
Características e benefícios
- Reactive groups: NHS ester (both ends)
- Reactive towards: amino groups (primary amines)
- Soluble in DMSO or DMF at a concentration of ~10 mM (3 mg/mL)
- Cleavable by sodium meta-periodate (Part No. 20504)
- Ideal for applications in which crosslink cleavability is desired without disturbing protein disulfide bonds
Atenção
This product is sensitive to moisture. The vial is packaged in a resealable bag with a desiccant to reduce exposure to moisture. After cold storage, equilibrate the vial to room temperature before opening to reduce condensation inside the vial. Make fresh solutions. Storage of stock solutions is not recommended. After use, return the vial to the resealable bag. Close the bag and store the product at the recommended temperature.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Certificados de análise (COA)
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Journal of immunology (Baltimore, Md. : 1950), 142(3), 842-847 (1989-02-01)
Properdin (P) is synthesized by the human promyelocytic cell line, HL-60, after differentiation with DMSO. The secreted P was physiochemically indistinguishable from purified plasma P. It was polymerized and able to bind to C3IBb-Sepharose but not to C3i-Sepharose. No extracellular
R J Smith et al.
Biochemistry, 17(18), 3719-3723 (1978-09-05)
Two novel cross-linkers, disuccinimidyl tartarate (DST) and N,N'-bis(3-succinimidyloxycarbonylpropyl)tartaramide (SPT), have been synthesized. These reagents span 6 and 18 A, respectively, between functional groups and contain a vic-glycol bond which can be cleaved with periodate under mild reaction conditions. Both DST
J Carlsson et al.
The Biochemical journal, 173(3), 723-737 (1978-09-01)
A heterobifunctional reagent, N-succinimidyl 3-(2-pyridyldithio)propionate, was synthesized. Its N-hydroxysuccinimide ester group reacts with amino groups and the 2-pyridyl disulphide structure reacts with aliphatic thiols. A new thiolation procedure for proteins is based on this reagent. The procedure involves two steps.
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