A3256
L-(+)-Arabinose
≥99% (GC)
Synonym(s):
(+)-Arabinose
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About This Item
Empirical Formula (Hill Notation):
C5H10O5
CAS Number:
Molecular Weight:
150.13
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
226-214-6
Beilstein/REAXYS Number:
1723085
MDL number:
Quality Level
assay
≥99% (GC)
form
powder
optical activity
[α]/D +103 to +105°°(lit.)
technique(s)
flow cytometry: suitable, gas chromatography (GC): suitable, ion chromatography: suitable, microbiological culture: suitable
color
white to off-white
mp
160-163 °C (lit.)
solubility
water: 100 mg/mL, clear, colorless
suitability
suitable for determination of protein concentration, suitable for microtiter plates
application(s)
genomic analysis
life science and biopharma
microbiology
SMILES string
OC[C@H](O)[C@H](O)[C@@H](O)C=O
InChI
1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4-,5+/m0/s1
InChI key
PYMYPHUHKUWMLA-VAYJURFESA-N
General description
L-(+)-Arabinose, a five-carbon sugar found widely in nature, plays a pivotal role in biochemical research, particularly in microbiology and biomedicine. In microbial culture, it serves as a sole carbon source for various bacteria, as many bacteria contain an inducible arabinose operon, allowing them to utilize L-arabinose as a primary carbon source. This characteristic has made arabinose indispensable in microbiological tests, including the arabinose test, which assesses a microbe′s ability to ferment arabinose.Beyond microbiology, L-arabinose has gained significance in the biomedicine industry due to its potential in drug delivery and metabolic disorder research, particularly in the treatment of conditions like diabetes. This natural sugar shows promise in regulating blood glucose levels and possesses antimicrobial properties, making it a subject of investigation in the fight against bacterial infections. Additionally, L-arabinose is utilized in protein expression studies, serving as a one-way switch for regulating gene expression.
Application
L-Arabinose has been used
- to induce and regulate the expression of specific genes or proteins in bacterial strains
L-Arabinose can be used as a substrate to identify, differentiate and characterize pentose sugar isomerase(s) and in the bioproduction of L-ribose.
Biochem/physiol Actions
L-Arabinose is the naturally occurring isomer and is a constituent of plant polysaccharides. Most bacteria contain an inducible arabinose operon that codes for a series of enzymes and transporters that allows L-arabinose to be used as the sole carbon source in microbial culture.
Features and Benefits
- Suitable for biochemical and cell culture research
- Versatile and adaptable for wide variety of laboratory and research applications
Other Notes
For additional information on our range of Biochemicals, please complete this form.
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
涉药品监管产品
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Wolf-Dieter Reiter
Current opinion in plant biology, 11(3), 236-243 (2008-05-20)
During the past few years, substantial progress has been made to understand the enzymology and regulation of nucleotide sugar interconversion reactions that are irreversible in vivo on thermodynamic grounds. Feedback inhibition of enzymes by metabolic end products appears to be
Wei Lin et al.
Molecular cell, 70(1), 60-71 (2018-04-03)
Fidaxomicin is an antibacterial drug in clinical use for treatment of Clostridium difficile diarrhea. The active ingredient of fidaxomicin, lipiarmycin A3 (Lpm), functions by inhibiting bacterial RNA polymerase (RNAP). Here we report a cryo-EM structure of Mycobacterium tuberculosis RNAP holoenzyme in
Koen J T Venken et al.
Nucleic acids research, 36(18), e114-e114 (2008-08-05)
Studying gene function in the post-genome era requires methods to localize and inactivate proteins in a standardized fashion in model organisms. While genome-wide gene disruption and over-expression efforts are well on their way to vastly expand the repertoire of Drosophila
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A3256-100G | 04061835366057 |
| A3256-10MG | 04061835366064 |
| A3256-1KG | 04061835366071 |
| A3256-25G | 04061835366088 |
| A3256-500G | 04061835366095 |