α-Factor Mating Pheromone, yeast
CAS No. 59401-28-4
α-Factor Mating Pheromone, yeast( Mating Factor α )
Catalog No. M29805 CAS No. 59401-28-4
Alpha factor mating pheromone is a peptide of 13 amino acids secreted by Saccharomyces cerevisiae α cells.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product Nameα-Factor Mating Pheromone, yeast
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NoteResearch use only, not for human use.
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Brief DescriptionAlpha factor mating pheromone is a peptide of 13 amino acids secreted by Saccharomyces cerevisiae α cells.
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DescriptionAlpha factor mating pheromone is a peptide of 13 amino acids secreted by Saccharomyces cerevisiae α cells. (In Vitro):α-Factor Mating Pheromone, yeast is synthesized constitutively by MATα cells and acting on MATa cells. α-Factor Mating Pheromone, yeast inhibits the division cycle of yeast a cells, and competes for binding of 35S-α-factor to haploid a cells, with Kd of 0.3 μM, and this binding is related to five temperature-sensitive ste2 mutants, and is thermolabile. However, α-Factor Mating Pheromone, yeast binding activity of other temperature-sensitive mutants (ste4, ste5, ste7, ste11, and ste12) shows no thermolability.
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In Vitroα-Factor Mating Pheromone, yeast is synthesized constitutively by MATα cells and acting on MATa cells. α-Factor Mating Pheromone, yeast inhibits the division cycle of yeast a cells, and competes for binding of 35S-α-factor to haploid a cells, with Kd of 0.3 μM, and this binding is related to five temperature-sensitive ste2 mutants, and is thermolabile. However, α-Factor Mating Pheromone, yeast binding activity of other temperature-sensitive mutants (ste4, ste5, ste7, ste11, and ste12) shows no thermolability.
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In Vivo——
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SynonymsMating Factor α
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PathwayOthers
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TargetOther Targets
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RecptorSte2p
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Research Area——
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Indication——
Chemical Information
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CAS Number59401-28-4
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Formula Weight1684
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Molecular FormulaC82H114N20O17S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : 50 mg/mL (29.69 mM)
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SMILES——
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Chemical NameSequence:Trp-His-Trp-Leu-Gln-Leu-Lys-Pro-Gly-Gln-Pro-Met-Tyr
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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CPYPP
CPYPP is an inhibitor of DOCK2-Rac1 interaction. CPYPP binds to DOCK2 DHR-2 domain and inhibits the guanine nucleotide exchange factor (GEF) activity of DOCK2DHR-2 for Rac1 in a dose-dependent manner(IC50 : 22.8 μM).
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ACBI3
ACBI3 (compound 7), a pan-KRAS degrader, effectively accomplishes the in vivo degradation of oncogenic KRAS .
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Compound K
HIV-IN-11 is part of the hydroxylaminoglutaramide (HAPA) transition state isomeric series of HIV protease inhibitors and is a potent and selective inhibitor of HIV-1 protease. HIV-IN-11 competitively inhibits HIV-1 PR (Ki: 0.049 nM) and potently inhibits replication of HIV(IIIb)-infected MT4 lymphocytes at concentrations of 25.0-50.0 nM. HIV-IN-11 displays a longer half-life than indinavir sulfate in animal models and serves as a promising second-generation HIV protease inhibitor.
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