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Supelco

HPLC peptide standard mixture

analytical standard

Synonym(s):

Peptide calibration standard for HPLC

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About This Item

UNSPSC Code:
85151701
NACRES:
NA.24

grade

analytical standard

Quality Level

200

description

Peptide standard

form

powder

composition

angiotensin II
Gly-Tyr
Leu enkephalin
Met enkephalin
Val-Tyr-Val

analyte chemical class(es)

amino acids, peptides, proteins

concentration

~0.5 mg each component (dried film)

technique(s)

HPLC: suitable

color

white

application(s)

food and beverages

compatibility

use to QA Reversed phase columns

format

multi-component solution

storage temp.

−20°C

Application

HPLC peptide standard mixture has been used for the separation of peptides of proteins in fish plasma samples using liquid chromatography coupled with quadrupole time of flight mass spectrometer (Q-TOF-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Amber vials containing a dried film composed of approx. 0.5 mg each of Gly-Tyr, Val-Tyr-Val, methionine enkephalin, leucine enkephalin and angiotensin II.

related product

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000288649
0000294636
0000283694
SLCP9303
SLCJ8598

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Simmons.D.BD and Sherry.PJ
Comparative Biochemistry and Physiology. Part D, Genomics & Proteomics, 19, 181-189 (2016)
Bob W J Pirok et al.
Journal of chromatography. A, 1530, 104-111 (2017-11-18)
Computer-aided method-development programs require accurate models to describe retention and to make predictions based on a limited number of scouting gradients. The performance of five different retention models for hydrophilic-interaction chromatography (HILIC) is assessed for a wide range of analytes.
Evelyn N Gitau et al.
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A global proteomic strategy was used to identify proteins, which are differentially expressed in the murine model of severe malaria in the hope of facilitating future development of novel diagnostic, disease monitoring and treatment strategies. Mice (4-week-old CD1 male mice)
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Dynamic pH barrage junction focusing in CE enables effective signal enhancement, quantitative capture efficiencies, and straightforward optimization. The method is a technical variant of dynamic pH junction focusing. CE separation with dynamic pH barrage junction focusing is compatible with both
Kanaka Hettiarachchi et al.
Journal of pharmaceutical and biomedical analysis, 176, 112794-112794 (2019-08-23)
The drive for faster separations while maintaining quality and yield remains an important consideration for enhanced productivity as well as cost reduction for drug discovery laboratories in the pharmaceutical industry. High-throughput experimentation (HTE) and high-throughput screening (HTS) techniques can benefit
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