QBD11102
Biotin-dPEG®11-oxyamine HCl
Manufacturer: Sigma Aldrich
Synonym(S): Polyethylene glycol
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 50 MG | QBD11102-50-MG | In Stock | ₹ 14,819.43 |
| 1000 MG | QBD11102-1000-MG | In Stock | ₹ 1,40,605.93 |
QBD11102 - 50 MG
In Stock
Quantity
1
Base Price: ₹ 14,819.43
GST (18%): ₹ 2,667.497
Total Price: ₹ 17,486.927
Assay
>90%
form
solid or viscous liquid
reaction suitability
reaction type: Biotinylationsreagent type: cross-linking reagent
polymer architecture
shape: linearfunctionality: monofunctional
shipped in
ambient
storage temp.
−20°C
SMILES string
O=C(CCCCC1SCC(N2)C1NC2=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO[NH3+].[Cl-]
Related Products
Description
- Features and Benefits: Biotin-dPEG®11-oxyamine.HCl allows biotin labeling of molecules with free aldehydes or ketones. This reagent is highly useful for labeling carbohydrates, glycoproteins, and other molecules with biotin following oxidation of the carbohydrate or glycan with sodium periodate or by chemical installation of an aldehyde or ketone on the target molecule. The dPEG® spacer is a single molecular weight PEG (44.9 Å) that provides excellent water solubility while extending the biotin moiety away from the surface of the labeled molecule for enhanced binding to avidin or streptavidin.
- Legal Information: Products Protected under U.S. Patents # 7,888,536 B2
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Assay: >90%
form: solid or viscous liquid
reaction suitability: reaction type: Biotinylationsreagent type: cross-linking reagent
polymer architecture: shape: linearfunctionality: monofunctional
shipped in: ambient
storage temp.: −20°C
SMILES string: O=C(CCCCC1SCC(N2)C1NC2=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO[NH3+].[Cl-]
Assay:
>90%
form:
solid or viscous liquid
reaction suitability:
reaction type: Biotinylationsreagent type: cross-linking reagent
polymer architecture:
shape: linearfunctionality: monofunctional
shipped in:
ambient
storage temp.:
−20°C
SMILES string:
O=C(CCCCC1SCC(N2)C1NC2=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO[NH3+].[Cl-]
Assay: >90%
form: solid or viscous liquid
reaction suitability: reactivity: thiol reactivereagent type: cross-linking reagentreactivity: amine reactive
polymer architecture: shape: linearfunctionality: heterobifunctional
shipped in: ambient
storage temp.: −20°C
SMILES string: O=C(CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCON1C(C2=C(C1=O)C=CC=C2)=O)ON3C(CCC3=O)=O
Assay:
>90%
form:
solid or viscous liquid
reaction suitability:
reactivity: thiol reactivereagent type: cross-linking reagentreactivity: amine reactive
polymer architecture:
shape: linearfunctionality: heterobifunctional
shipped in:
ambient
storage temp.:
−20°C
SMILES string:
O=C(CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCON1C(C2=C(C1=O)C=CC=C2)=O)ON3C(CCC3=O)=O
Assay: >90%
form: solid or viscous liquid
reaction suitability: reagent type: chelatorreagent type: cross-linking reagent
polymer architecture: shape: linearfunctionality: monofunctional
shipped in: ambient
storage temp.: −20°C
SMILES string: __
Assay:
>90%
form:
solid or viscous liquid
reaction suitability:
reagent type: chelatorreagent type: cross-linking reagent
polymer architecture:
shape: linearfunctionality: monofunctional
shipped in:
ambient
storage temp.:
−20°C
SMILES string:
__
Assay: >90%
form: solid or viscous liquid
reaction suitability: reagent type: chelatorreagent type: cross-linking reagentreagent type: fluorescent-labelling reagent
polymer architecture: shape: linearfunctionality: monofunctional
shipped in: ambient
storage temp.: −20°C
SMILES string: O=C(CN1CCN(CCN(CCN(CC1)CC(NCCOCCOCCOCCOCCC(OC2=C(C(F)=CC(F)=C2F)F)=O)=O)CC(OC(C)(C)C)=O)CC(OC(C)(C)C)=O)OC(C)(C)C
Assay:
>90%
form:
solid or viscous liquid
reaction suitability:
reagent type: chelatorreagent type: cross-linking reagentreagent type: fluorescent-labelling reagent
polymer architecture:
shape: linearfunctionality: monofunctional
shipped in:
ambient
storage temp.:
−20°C
SMILES string:
O=C(CN1CCN(CCN(CCN(CC1)CC(NCCOCCOCCOCCOCCC(OC2=C(C(F)=CC(F)=C2F)F)=O)=O)CC(OC(C)(C)C)=O)CC(OC(C)(C)C)=O)OC(C)(C)C