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Merck
CN

T6901

α1-Mating Factor acetate salt

≥93% (HPLC), synthetic

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About This Item

Empirical Formula (Hill Notation):
C82H114N20O17S
CAS Number:
Molecular Weight:
1683.97
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
51111800
MDL number:
Form:
powder
Assay:
≥93% (HPLC)
Biological source:
synthetic
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biological source

synthetic

Quality Level

assay

≥93% (HPLC)

form

powder

technique(s)

cell culture | mammalian: suitable

storage temp.

−20°C

SMILES string

CSCCC(NC(=O)C1CCCN1C(=O)C(CCC(N)=O)NC(=O)CNC(=O)C2CCCN2C(=O)C(CCCCN)NC(=O)C(CC(C)C)NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(Cc3c[nH]c4ccccc34)NC(=O)C(Cc5cnc[nH]5)NC(=O)C(N)Cc6c[nH]c7ccccc67)C(=O)NC(Cc8ccc(O)cc8)C(O)=O

InChI

1S/C82H114N20O17S/c1-45(2)34-61(98-76(112)63(38-49-41-89-56-17-9-7-15-53(49)56)99-77(113)64(39-50-42-87-44-91-50)96-71(107)54(84)37-48-40-88-55-16-8-6-14-52(48)55)74(110)93-57(25-27-68(85)104)72(108)97-62(35-46(3)4)75(111)95-59(18-10-11-30-83)80(116)101-31-12-19-66(101)78(114)90-43-70(106)92-60(26-28-69(86)105)81(117)102-32-13-20-67(102)79(115)94-58(29-33-120-5)73(109)100-65(82(118)119)36-47-21-23-51(103)24-22-47/h6-9,14-17,21-24,40-42,44-46,54,57-67,88-89,103H,10-13,18-20,25-39,43,83-84H2,1-5H3,(H2,85,104)(H2,86,105)(H,87,91)(H,90,114)(H,92,106)(H,93,110)(H,94,115)(H,95,111)(H,96,107)(H,97,108)(H,98,112)(H,99,113)(H,100,109)(H,118,119)

InChI key

SBKVPJHMSUXZTA-UHFFFAOYSA-N

Application

α1-Mating Factor acetate salt has been used for the synchronization of yeast cells for flow cytometry and to study B-type cyclin (Clb2p)-EmCitrine levels from calcofluor white treated cells.

Biochem/physiol Actions

The α1-Mating factor is a pheromone produced by yeast that regulates mating. α1-Mating Factor acetate salt can be utilized to arrest the G1-phase of the cell cycle in various yeast strains.

Preparation Note

Alpha1-Mating Factor acetate salt dissolves in water at 1 mg/ml to yield a clear, colorless solution.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

涉药品监管产品

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C Formosa et al.
Journal of molecular recognition : JMR, 28(1), 1-9 (2015-06-06)
Single-molecule force spectroscopy using atomic force microscopy (AFM) is more and more used to detect and map receptors, enzymes, adhesins, or any other molecules at the surface of living cells. To be specific, this technique requires antibodies or ligands covalently
Christopher Ptak et al.
The Journal of cell biology, 220(12) (2021-11-18)
In eukaryotes, chromatin binding to the inner nuclear membrane (INM) and nuclear pore complexes (NPCs) contributes to spatial organization of the genome and epigenetic programs important for gene expression. In mitosis, chromatin-nuclear envelope (NE) interactions are lost and then formed
Christian Hoffmann et al.
Methods in molecular biology (Clifton, N.J.), 1728, 247-262 (2018-02-07)
The installation of unnatural amino acids into proteins of living cells is an enabling technology that facilitates an enormous number of applications. UV-activatable crosslinker amino acids allow the formation of a covalent bond between interaction partners in living cells with
Brianna L Greenwood et al.
Methods in molecular biology (Clifton, N.J.), 2579, 145-168 (2022-09-01)
The cell division cycle is a fundamental process required for proliferation of all living organisms. The eukaryotic cell cycle follows a basic template with an ordered series of events beginning with G1 (Gap1) phase, followed successively by S (Synthesis) phase
Yasmin Lau et al.
Current biology : CB, 32(5), 963-974 (2022-01-28)
Prion-like proteins are involved in many aspects of cellular physiology, including cellular memory. In response to deceptive courtship, budding yeast escapes pheromone-induced cell-cycle arrest through the coalescence of the G1/S inhibitor Whi3 into a dominant, inactive super-assembly. Whi3 is a

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Product Information Sheet

Global Trade Item Number

SKUGTIN
T6901-5MG04061837372155
T6901-.5MG04061837372131
T6901-1MG04061837372148

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