Human/Rat/Mouse/Pig/Chicken/Frog Somatostatin 14 Protein

Human/Rat/Mouse/Pig/Chicken/Frog Somatostatin 14 Protein

Cat. No.: DPP-001178

Size: 50 µg Size: 100 µg Size: Costomer Size
Product Overview
Species Human, Rat, Mouse, Pig, Chicken, Frog
Format Lyophilized
Purity ≥ 95% by Densitometry
Target Information
UniProt No. P61278; P60042; P60041; P01168; O46688; F1MV99
Molecular Formula C76H104N18O19S2
Molecular Weight 1638
Function Somatostatin [SST, GHIH (growth hormone-inhibiting hormone) or SRIF (somatotropin release-inhibiting factor)] is a cyclic peptide hormone existing as two isoforms and produced in the pancreas islet, GI tract and the central nervous system. Tetradecapeptide Somatostatin-14 (SRIF-14, the originally identified somatostatin) and the 28-amino acid Somatostatin-28 (SRIF-28) have similar biological activities but differ in their potency. Somatostatins regulate the endocrine system: they inhibit the release of growth hormone in contrast to Growth Hormone Factor (GRF), which stimulates the release of growth hormone. They also inhibit the release of prolactin and thyrotropin, peptide hormones from the pituitary gland and glucagon and insulin from the pancreas. They control the secretion of gut hormones and function as neurotransmitters.
Sequence AGCKNFFWKTFTSC (Disulfide bridge: 3-14)
Sequence H-Ala-Gly-Cys-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Thr-Ser-Cys-OH (Disulfide bridge: 3-14)
Shipping & Storage
Shipping Shipped on dry ice.
Storage Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.
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Ace Therapeutics has a team of experts in the field of endocrine and metabolic research, aiming to provide innovative preclinical contract research solutions to cope with diabetes and its complications. We provide customized solutions and technical support, enabling the transformation of promising concepts into innovative treatments, thus accelerating the drug development process of diabetes.

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