logo
AAT Bioquest

bBBr [Dibromobimane] *CAS 68654-25-1*

dBBr is one of the most popular thiol-reactive fluorescent tags, and is widely used to detect various thiol-containing biomolecules such as glutathione in cells. It is fluorogenic upon reacting with thiol-containing molecules. Dibromobimane is a unique fluorogenic crosslinking reagent for proteins because it is unlikely to fluoresce until both of its alkylating groups have reacted. It has been used to crosslink thiols in myosin, hemoglobin, Escherichia coli lactose permease and mitochondrial ATPase. Dibromobimane is also used to probe for the proximity of dual-cysteine mutagenesis sites in ArsA ATPase and to crosslink thiols in actin, myosin and P-glycoprotein.
Product Image
Product Image
Gallery Image 1
Ordering information
Price
Unit size
Catalog Number634
Quantity
Add to cart
Additional ordering information
Telephone1-800-990-8053
Fax1-800-609-2943
Emailsales@aatbio.com
InternationalSee distributors
Bulk requestInquire
Custom sizeInquire
ShippingStandard overnight for United States, inquire for international
Request quotation
Physical properties
Molecular weight350.01
SolventDMSO
Spectral properties
Excitation (nm)394
Emission (nm)490
Storage, safety and handling
H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22
StorageFreeze (< -15 °C); Minimize light exposure
UNSPSC12171501
CAS68654-25-1
Calculators

Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of bBBr [Dibromobimane] *CAS 68654-25-1* to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.

0.1 mg0.5 mg1 mg5 mg10 mg
1 mM285.706 µL1.429 mL2.857 mL14.285 mL28.571 mL
5 mM57.141 µL285.706 µL571.412 µL2.857 mL5.714 mL
10 mM28.571 µL142.853 µL285.706 µL1.429 mL2.857 mL

Molarity calculator

Enter any two values (mass, volume, concentration) to calculate the third.

Mass (Calculate)Molecular weightVolume (Calculate)Concentration (Calculate)Moles
/=x=
Spectrum
References
View all 25 references: Citation Explorer
Reactivity of zinc finger cysteines: chemical modifications within labile zinc fingers in estrogen receptor
Authors: Atsriku C, Scott GK, Benz CC, Baldwin MA.
Journal: J Am Soc Mass Spectrom (2005): 2017
Interaction of S100A8/S100A9-arachidonic acid complexes with the scavenger receptor CD36 may facilitate fatty acid uptake by endothelial cells
Authors: Kerkhoff C, Sorg C, T and on NN, Nacken W.
Journal: Biochemistry (2001): 241
Determination of plasma homocysteine by high performance liquid chromatography with fluorescence detection
Authors: Liao Y, Liang YQ, Zhi XM, Liao ZH.
Journal: Se Pu (2000): 49
Plasma cysteine deficiency and decreased reduction of nitrososulfamethoxazole with HIV infection
Authors: Naisbitt DJ, Vilar FJ, Stalford AC, Wilkins EG, Pirmohamed M, Park BK.
Journal: AIDS Res Hum Retroviruses (2000): 1929
Fatty acid translocase/CD36 mediates the uptake of palmitate by type II pneumocytes
Authors: Guthmann F, Haupt R, Looman AC, Spener F, Rustow B.
Journal: Am J Physiol (1999): L191