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Merck
CN

5000

Oxaloacetic Acid - CAS 328-42-7 - Calbiochem

Substrate for malate dehydrogenase and oxaloacetate decarboxylase.

Synonym(s):

Oxaloacetic Acid - CAS 328-42-7 - Calbiochem, OAA

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About This Item

Empirical Formula (Hill Notation):
C4H4O5
CAS Number:
Molecular Weight:
132.07
UNSPSC Code:
12352200
MDL number:
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Quality Level

assay

>98% (titration)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze

color

white to off-white

solubility

water: soluble

shipped in

ambient

storage temp.

2-8°C

InChI

1S/C4H4O5/c5-2(4(8)9)1-3(6)7/h1H2,(H,6,7)(H,8,9)

InChI key

KHPXUQMNIQBQEV-UHFFFAOYSA-N

General description

Substrate for malate dehydrogenase and oxaloacetate decarboxylase.

Preparation Note

Following reconstitution, refrigerate (4°C).

Other Notes

Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
Flint, D.H. 1993. Biochemistry 32, 799.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Corrosive (L)

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2

Storage Class

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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Heather C Rice et al.
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The amyloid-β (Aβ) peptide, the primary constituent of amyloid plaques found in Alzheimer's disease (AD) brains, is derived from sequential proteolytic processing of the Amyloid Precursor Protein (APP). However, the contribution of different cell types to Aβ deposition has not
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5-Methylcytosine (m5C) is a prevalent base modification in tRNA and rRNA but it also occurs more broadly in the transcriptome, including in mRNA, where it serves incompletely understood molecular functions. In pursuit of potential links of m5C with mRNA translation
Gabriel Crevier-Sorbo et al.
Acta neuropathologica communications, 8(1), 14-14 (2020-02-09)
Huntington's disease (HD) is an autosomal dominant trinucleotide repeat disorder characterized by choreiform movements, dystonia and striatal neuronal loss. Amongst multiple cellular processes, abnormal neurotransmitter signalling and decreased trophic support from glutamatergic cortical afferents are major mechanisms underlying striatal degeneration.

Global Trade Item Number

SKUGTIN
880123P-500UG04061835192311
880132P-10MG04061835192335
880227P-10MG04061835192373
880123X-500UG04061837668227
880224P-5MG04061835192359
880226P-5MG04061835192366
880224C-5MG04061837668449
8920-50004053252621178
81834204061833508480
17359-1G-F04061826661611
BR704652-25EA04061831866728
EP311011200804065270495679
EP3110112008-1EA04022536210100
671266-500MG04061833549445
671266-100MG04061833466636
EPM1196-9902-1EA04061835088263

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