Chemerin-9 (149-157)
CAS No. 676367-27-4
Chemerin-9 (149-157)( —— )
Catalog No. M30316 CAS No. 676367-27-4
The nonapeptide 149,YFPGQFAFS157 (chemerin-9), corresponding to the C terminus of processed chemerin, retained most of the activity of the full-size protein, with regard to agonism toward the chemerinR.the natural ligand of ChemR23 (chemerinR).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
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Biological Information
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Product NameChemerin-9 (149-157)
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NoteResearch use only, not for human use.
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Brief DescriptionThe nonapeptide 149,YFPGQFAFS157 (chemerin-9), corresponding to the C terminus of processed chemerin, retained most of the activity of the full-size protein, with regard to agonism toward the chemerinR.the natural ligand of ChemR23 (chemerinR).
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DescriptionThe nonapeptide 149,YFPGQFAFS157 (chemerin-9), corresponding to the C terminus of processed chemerin, retained most of the activity of the full-size protein, with regard to agonism toward the chemerinR.the natural ligand of ChemR23 (chemerinR).
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In VitroChemerin-9 (149-157) (0.1 nM; 24 h; cardiac fibroblasts) stimulates migration in cardiac fibroblasts and stimulates phosphorylation of Akt and ERK as well as ROS production. Western Blot Analysis Cell Line:Cardiac fibroblasts Concentration:0.1 nM Incubation Time:24 hours Result:Stimulated phosphorylation of Akt and ERK.
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In VivoChemerin-9 (149-157) (0.2 mg/kg; i.p.; daily, for 42 days) alleviates glucose intolerance and IR in PDM mice.Chemerin-9 (149-157) (7.7? μg /kg; i.h.; daily, for 28 days) has anti-inflammatory and anti-angiogenic effects in ApoE-/- mice and protects the abdominal aorta from MMP damage.Chemerin-9 (149-157) (8 μg/kg; ICV; daily; for 14 d; male Kunming mice) ameliorates Aβ1-42-induced memory impairment. Animal Model:PDM mice Dosage:0.2 mg/kg Administration:Intraperitoneal injection; daily, for 42 daysResult:Increased expression of chemerin, GLUT2, and PDX1, which led to the alleviation of glucose intolerance and IR in PDM model mice. Animal Model: ApoE-/- mice Dosage:7.7 μg /kg Administration:Subcutaneous injection; daily, for 28 days Result:Suppressed the enlargement of abdominal aorta and reversed the SMC loss.Animal Model:ApoE-/- mice Dosage:7.7 μg/kg Administration:Subcutaneous injection; daily, for 28 days Result:Down-regulated MMP2 and MMP-9 expression and decreased the levels of chemerin and CMKLR1.Animal Model:Male Kunming mice Dosage:8 μg/kg Administration:Intracerebroventrical injection; daily; for 14 days Result:Increased in the levels of pro-in?ammatory cytokines such as interleukin-1β (IL-1β), tumor necrosis factor (TNF-α) and interleukin-6 (IL-6) in the hippocampus.
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Synonyms——
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PathwayMembrane Transporter/Ion Channel
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TargetBeta Amyloid
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number676367-27-4
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Formula Weight1063.16
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Molecular FormulaC54H66N10O13
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Purity>98% (HPLC)
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Solubility——
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SMILES——
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Chemical NameSequence:{Tyr}{Phe}{Pro}{Gly}{Gln}{Phe}{Ala}{Phe}{Ser}
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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β-Amyloid 13-27
β-Amyloid (13-27) is a peptide consisting of amino acid of 13 to 27 of beta amyloid protein. This synthetic peptide consists of amino acids 26 to 40 of beta amyloid protein. It can be used to study the kinetics of beta amyloid formation.
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Sophoridine
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