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Catalog Number:
21004
CAS Number:
129787-67-3
5-Bromo-4-chloro-3-indoxyl-β-D-mannopyranoside
Synonym(s):
X-β-D-mannoside
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Product Information

5-Bromo-4-chloro-3-indoxyl-β-D-mannopyranoside is a versatile compound widely utilized in biochemical research and applications. This compound serves as a chromogenic substrate for the detection of β-galactosidase, making it invaluable in molecular biology and microbiology. Its unique structure allows for the visualization of enzyme activity, facilitating the study of gene expression and enzyme kinetics in various organisms. Researchers appreciate its ability to produce a distinct color change upon enzymatic reaction, which enhances the accuracy of assays and experiments.

In addition to its applications in enzyme assays, 5-Bromo-4-chloro-3-indoxyl-β-D-mannopyranoside is also employed in histochemical staining techniques, aiding in the identification of specific cell types and biological processes. Its stability and ease of use make it a preferred choice among professionals in laboratories focused on genetic research, diagnostics, and pharmaceutical development. By incorporating this compound into their workflows, researchers can achieve reliable results and gain deeper insights into cellular functions and enzyme activities.

Synonyms
X-β-D-mannoside
CAS Number
129787-67-3
Molecular Formula
C14H15BrClNO6
Molecular Weight
408.63
MDL Number
MFCD07779478
PubChem ID
619018
Conditions
Conserver à 0-8°C
General Information
Synonyms
X-β-D-mannoside
CAS Number
129787-67-3
Molecular Formula
C14H15BrClNO6
Molecular Weight
408.63
MDL Number
MFCD07779478
PubChem ID
619018
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

5-Bromo-4-chloro-3-indoxyl-b-D-mannopyranoside is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in enzyme assays, particularly for detecting β-galactosidase activity, which is crucial in various biological studies.
  • Histochemical Staining: It is employed in histochemistry for visualizing specific enzyme activities in tissue samples, aiding pathologists and researchers in diagnosing diseases.
  • Plant Research: The compound is used to study gene expression in plants, allowing researchers to understand metabolic pathways and plant responses to environmental changes.
  • Microbial Studies: It acts as a selective marker in microbiology, helping in the identification of genetically modified organisms by indicating successful gene integration.
  • Drug Development: This chemical is valuable in pharmaceutical research for screening potential drug candidates, particularly those targeting glycosylation processes.

Citations