Y1625
Yeast Extract
for use in microbial growth medium
동의어(들):
Select Yeast Extract, microbial growth media, microbial growth medium
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
CAS 번호:
UNSPSC Code:
41106212
eCl@ss:
42040000
EC Number:
232-387-9
NACRES:
NA.85
MDL number:
SMILES string
OC(=O)CC1c2c3c(ccc2c4c1cccc4)cccc3
InChI
1S/C19H14O2/c20-18(21)11-17-15-8-4-3-7-14(15)16-10-9-12-5-1-2-6-13(12)19(16)17/h1-10,17H,11H2,(H,20,21)
InChI key
GQNBDGXKDJSVGQ-UHFFFAOYSA-N
grade
Molecular Biology
sterility
non-sterile
form
powder
technique(s)
microbiological culture: suitable using
application(s)
agriculture
storage temp.
room temp
suitability
nonselective for Escherichia coli, nonselective for coliforms
Quality Level
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General description
Yeast extract is produced by various yeast species mainly by Saccharomyces cerevisiae or baker’s yeast. In addition to its use as a supplement in culture media for microbial research and biotechnology, yeast extract is also used as a component of the complex media for industrial fermentations.It also serves as a nutritional source for various microbial media.
Application
For general bacteriological use with a variety of microorganisms.
Yeast Extract has been used as a component of:
- complex media for culturing E. coli clones for shake flask experiments
- culture media for culturing bacterial species Gluconacetobacter xylinus
- yeast extract beef (YEB) media for the transformation of Agrobacterium
Yeast extract is used as a bacteriological media component for a variety of microorganisms and molecular genetics applications.
Other Notes
Water soluble portion of autolyzed yeast with intact B-complex vitamins. Yeast extract is a mixture of amino acids, peptides, water soluble vitamins and carbohydrates and can be used as additive for culture media.
저장 등급
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Luciana M Katiki et al.
Veterinary parasitology, 182(2-4), 264-268 (2011-06-18)
The most challenging obstacles to testing products for their anthelmintic activity are: (1) establishing a suitable nematode in vitro assay that can evaluate potential product use against a parasitic nematode of interest and (2) preparation of extracts that can be
Carolina Fernandez-Senac et al.
Journal of fish diseases, 43(11), 1463-1472 (2020-09-04)
Routine gill swabbing is a non-destructive sampling method used for the downstream qPCR detection and quantitation of the pathogen Neoparamoeba perurans, a causative agent of amoebic gill disease (AGD). Three commercially available swabs were compared aiming their application for timelier
Lucija Markulin et al.
Planta, 250(1), 347-366 (2019-05-01)
The involvement of a WRKY transcription factor in the regulation of lignan biosynthesis in flax using a hairy root system is described. Secoisolariciresinol is the main flax lignan synthesized by action of LuPLR1 (pinoresinol-lariciresinol reductase 1). LuPLR1 gene promoter deletion
Pascal Chatonnet et al.
Journal of agricultural and food chemistry, 58(23), 12481-12490 (2010-11-10)
This study identifies a previously isolated bacterium as Rhizobium excellensis, a new species of proteobacteria able to form a large quantity of 2-methoxy-3,5-dimethylpyrazine (MDMP). R. excellensis actively synthesizes MDMP from L-alanine and L-leucine and, to a lesser extent, from L-phenylalanine
Benjamin A Adducci et al.
Biosensors & bioelectronics, 78, 160-166 (2015-11-26)
New methods and technology are needed to quickly and accurately detect potential biological warfare agents, such as Bacillus anthracis, causal agent of anthrax in humans and animals. Here, we report the detection of a simulant of B. anthracis (B. globigii)
프로토콜
TE Buffer; Elution Buffer; 10x Ligation Buffer; 0.5 M PIPES Buffer; Inoue Transformation Buffer
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