SLLK, Control Peptide for TSP1 Inhibitor

Modify Date: 2024-01-08 23:28:40

SLLK, Control Peptide for TSP1 Inhibitor Structure
SLLK, Control Peptide for TSP1 Inhibitor structure
Common Name SLLK, Control Peptide for TSP1 Inhibitor
CAS Number 464924-27-4 Molecular Weight 459.580
Density 1.3±0.1 g/cm3 Boiling Point 690.1±65.0 °C at 760 mmHg
Molecular Formula C21H41N5O6 Melting Point N/A
MSDS N/A Flash Point 371.2±34.3 °C

 Use of SLLK, Control Peptide for TSP1 Inhibitor


SLLK, Control Peptide for TSP1 Inhibitor is a control peptide for LSKL (leucine-serine-lysine-leucine).

 Names

Name (2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-amino-1,3-dihydroxy-propylidene]amino]-1-hydroxy-4-methyl-pentylidene]amino]-1-hydroxy-4-methyl-pentylidene]amino]hexanoic acid

 SLLK, Control Peptide for TSP1 Inhibitor Biological Activity

Description SLLK, Control Peptide for TSP1 Inhibitor is a control peptide for LSKL (leucine-serine-lysine-leucine).
Related Catalog
In Vivo TGF-β1 is significantly lower (0.10±0.01 pg/mL) in the plasma of mice receiving LSKL compared with that in plasma of mice receiving SLLK control peptide at day 42 (0.20±0.02 pg/mL; P=0.0001). mRNA expression is assessed in the suprarenal aortic lysates obtained from mice receiving SLLK and LSKL peptides[1]. Akita mice treated with 30 mg/kg LSKL have significantly increased nephrin expression, greater than twofold, compared with renal lysates from either saline controls or SLLK-treated mice[2].
Animal Admin Sterile solutions of LSKL or SLLK peptide are made in stock solutions of 3.0 mg/mL (high dose) or 0.3 mg/mL (low dose) in sterile saline. The i.p. injection of LSKL, SLLK, or saline began 2 weeks after uninephrectomy and continues thrice weekly for 15 weeks. For the low-dosage treatment regimen, each group of 20 mice receives 3 mg/kg body weight of peptide (LSKL or SLLK) per injection or saline (100 μL/10 g body weight per injection). For the high-dosage treatment regimen, Akita mice ae given i.p. injections of LSKL or SLLK peptide at 30 mg/kg body weight per injection or saline (100 μL/10 g body weight per injection).
References

[1]. Krishna SM, et al. A peptide antagonist of thrombospondin-1 promotes abdominal aortic aneurysm progression in the angiotensin II-infused apolipoprotein-E-deficient mouse. Arterioscler Thromb Vasc Biol. 2015 Feb;35(2):389-98.

[2]. Lu A, et al. Blockade of TSP1-dependent TGF-β activity reduces renal injury and proteinuria in a murine model of diabetic nephropathy. Am J Pathol. 2011 Jun;178(6):2573-86.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 690.1±65.0 °C at 760 mmHg
Molecular Formula C21H41N5O6
Molecular Weight 459.580
Flash Point 371.2±34.3 °C
Exact Mass 459.305695
LogP 2.91
Vapour Pressure 0.0±4.9 mmHg at 25°C
Index of Refraction 1.565
Storage condition 2-8℃
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