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S1315

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L-Serin

Synonym(e):

(S)-(+)-2-Amino-3-hydroxy-propionsäure

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About This Item

Lineare Formel:
HOCH2CH(NH2)CO2H
CAS-Nummer:
56-45-1
Molekulargewicht:
105.09
Beilstein:
1721404
EG-Nummer:
200-274-3
MDL-Nummer:
MFCD00064224
UNSPSC-Code:
12352209

Biologische Quelle

non-animal source

Assay

≥98.5%

Hersteller/Markenname

Ajinomoto

Methode(n)

cell culture | mammalian: suitable

Verunreinigungen

endotoxin, tested

mp (Schmelzpunkt)

222 °C (dec.) (lit.)

Löslichkeit

H2O: 50 mg/mL

Eignung

suitable for manufacturing use

Anwendung(en)

pharmaceutical (small molecule)

SMILES String

N[C@@H](CO)C(O)=O

InChI

1S/C3H7NO3/c4-2(1-5)3(6)7/h2,5H,1,4H2,(H,6,7)/t2-/m0/s1

InChIKey

MTCFGRXMJLQNBG-REOHCLBHSA-N

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Allgemeine Beschreibung

To request documentation for this product, please contact Customer Support and select ‘Product Documentation′. Please note that access to documentation for this product requires a confidentiality disclosure agreement.

Anwendung

L-Serine is classified as a non-essential amino acid. It is used as a cell culture media component and raw material for the commercial biomanufacture of therapeutic recombinant proteins and monoclonal antibodies.

Biochem./physiol. Wirkung

Vorläufer von Glycin in der Serin-Hydroxymethyltransferase-Reaktion.

Anwendung

Produkt-Nr.
Beschreibung
Preisangaben

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Miyoshi Haruta et al.
Science (New York, N.Y.), 343(6169), 408-411 (2014-01-25)
Plant cells are immobile; thus, plant growth and development depend on cell expansion rather than cell migration. The molecular mechanism by which the plasma membrane initiates changes in the cell expansion rate remains elusive. We found that a secreted peptide
Kenji Hashimoto et al.
Progress in neuro-psychopharmacology & biological psychiatry, 29(5), 767-769 (2005-06-09)
Several lines of evidence suggest that D-serine, an endogenous agonist of the glycine site on the NMDA receptors, might play a role in the pathophysiology of schizophrenia. The purpose of this study was to determine whether levels of D- and
Vanessa A Morais et al.
Science (New York, N.Y.), 344(6180), 203-207 (2014-03-22)
Under resting conditions, Pink1 knockout cells and cells derived from patients with PINK1 mutations display a loss of mitochondrial complex I reductive activity, causing a decrease in the mitochondrial membrane potential. Analyzing the phosphoproteome of complex I in liver and
Chang-Ching Liu et al.
Molecular and cellular biology, 34(1), 57-70 (2013-10-30)
In budding yeast (Saccharomyces cerevisiae), the cell cycle-dependent telomere elongation by telomerase is controlled by the cyclin-dependent kinase 1 (Cdk1). The telomere length homeostasis is balanced between telomerase-unextendable and telomerase-extendable states that both require Cdc13. The recruitment of telomerase complex
Cedric Cagliero et al.
Nucleic acids research, 41(12), 6058-6071 (2013-05-02)
To fit within the confines of the cell, bacterial chromosomes are highly condensed into a structure called the nucleoid. Despite the high degree of compaction in the nucleoid, the genome remains accessible to essential biological processes, such as replication and
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Chromatograms

application for HPLC

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