HMBR
CAS No. 1287651-36-8
HMBR( —— )
Catalog No. M37102 CAS No. 1287651-36-8
HMBR are not fluorescent by themselves, but when combined with Y-FAST, they emit yellow light when excited by blue light.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 174 | In Stock |
|
| 10MG | 282 | In Stock |
|
| 25MG | 566 | In Stock |
|
| 50MG | 886 | In Stock |
|
| 100MG | 1414 | In Stock |
|
| 200MG | 1841 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameHMBR
-
NoteResearch use only, not for human use.
-
Brief DescriptionHMBR are not fluorescent by themselves, but when combined with Y-FAST, they emit yellow light when excited by blue light.
-
DescriptionHMBR, an analog bearing an additional methyl group on the aromatic ring, is nonfluorescent by itself, but it fluoresces yellow light upon blue-light excitation when bound to Y-FAST. HMBR is nontoxic for zebrafish embryos. cell-permeant.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1287651-36-8
-
Formula Weight251.32
-
Molecular FormulaC11H9NO2S2
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 125 mg/mL (497.37 mM; Ultrasonic (<80°C)
-
SMILESC(=C/1\SC(=S)NC1=O)\C2=CC(C)=C(O)C=C2
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Plamont MA, et al. Small fluorescence-activating and absorption-shifting tag for tunable protein imaging in vivo [published correction appears in Proc Natl Acad Sci U S A. 2016 Mar 8;113(10):E1412. Moncoq, Karine [added]]. Proc Natl Acad Sci U S A. 2016;113(3):497-502.?
molnova catalog
related products
-
4-(Dimethylamino)cin...
4-(Dimethylamino)cinnamic acid (DMACA) could be as charge transfer (ICT) probe.
-
(2E)-3-(3,5-dimethox...
(2E)-3-(3,5-dimethoxyphenyl)-1-(2-methoxyphenyl)prop-2-en-1-one is a chemical compound.
-
WDR5-0102
WDR5-0102 is a compound that inhibits the WDR5-MLL1 interface (K dis = 7 μM, K d = 4 μM), selectively reducing MLL1 HMT activity without affecting the human H3K4 methyltransferase SETD7 or other HMTs, including G9a, EHMT1, SUV39H2, SETD8, PRMT3, and PRMT5.
Cart
sales@molnova.com