Kisspeptin 234
mRNA synthesis
In vitro transcription of capped mRNA with modified nucleotides and Poly(A) tail
Tyramide Signal Amplification (TSA)
TSA (Tyramide Signal Amplification), used for signal amplification of ISH, IHC and IC etc.
Phos Binding Reagent Acrylamide
Separation of phosphorylated and non-phosphorylated proteins without phospho-specific antibody
Cell Counting Kit-8 (CCK-8)
A convenient and sensitive way for cell proliferation assay and cytotoxicity assay
SYBR Safe DNA Gel Stain
Safe and sensitive stain for visualization of DNA or RNA in agarose or acrylamide gels.
Inhibitor Cocktails
Protect the integrity of proteins from multiple proteases and phosphatases for different applications.
Kisspeptin 234 is a kisspeptin receptor antagonist, with the ability to antagonize kisspeptin-10-induced activation of gpr-54. Kisspeptin binds to its cognate receptor (i.e. gpr-54) on neurons that produce gonadotropin-releasing hormone (GnRH), and stimulates their activity, which in turn sends an obligatory signal for GnRH secretion, thereby gating down-stream events supporting reproduction. The development of kisspeptin receptor antagonists may provide a valuable tool for exploring the physiological and pathophysiological roles of kisspeptin in the regulation of reproduction, and could serve as a potential therapeutic agent for treating hormone-dependent disorders of reproduction, such as precocious puberty, endometriosis, as well as metastatic prostate cancer.
Reference:
1. Roseweir AK, Kauffman AS, Smith JT, et al. Discovery of potent kisspeptin antagonists delineate physiological mechanisms of gonadotropin regulation. Journal of Neuroscience, 2009, 29(12): 3920-3929.
Physical Appearance | White lyophilised solid |
Storage | Store at -20°C |
M.Wt | 1295.42 |
Cas No. | 1145998-81-7 |
Formula | C63H78N18O13 |
Solubility | insoluble in DMSO; insoluble in EtOH; ≥4.44 mg/mL in H2O with ultrasonic |
Chemical Name | (S,Z)-N'1-((6S,7Z,9R,10Z,13Z,15S,16Z,19Z,21S,22Z,24S)-9-((1H-indol-3-yl)methyl)-1-amino-15-benzyl-8,11,14,17,20,23-hexahydroxy-6-((Z)-hydroxy(((S)-1-hydroxy-1-imino-3-phenylpropan-2-yl)imino)methyl)-21-(2-hydroxy-2-iminoethyl)-1-imino-25-(1H-indol-3-yl)-2 |
SDF | Download SDF |
Canonical SMILES | C[C@](/N=C(O)/C)([H])/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/[C@@](/C(O)=N/C/C(O)=N/[C@@](/C(O)=N/C/C(O)=N/[C@](/C(O)=N/[C@@](/C(O)=N/[C@@](C(O)=N)([H])CC1=CC=CC=C1)([H])CCCNC(N)=N)([H])CC2=CNC3=CC=CC=C23)([H])CC4=CC=CC=C4)([H])CC(O)=N)([H])CC5=CNC6=CC=CC=C56 |
运输条件 | 蓝冰运输或根据您的需求运输。 |
一般建议 | 不同厂家不同批次产品溶解度各有差异,仅做参考。若实验所需浓度过大至产品溶解极限,请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存,请尽快用完。 |
Cell experiment:[1] | |
Cell lines |
GnRH neurons |
Reaction Conditions |
100 pM ~ 10 μM kisspeptin 234 |
Applications |
Kisspeptin 234 substantially inhibited kisspeptin-10 stimulation of inositol phosphate, with an IC50 value of 7 nM. At the doses of 1, 10 and 100 nM, kisspeptin 234 significantly reduced kisspeptin-10-induced GnRH neuron firing activity. |
Animal experiment:[1] | |
Animal models |
Pubertal female rhesus monkeys |
Dosage form |
10 nM Infusion of 10 nM kisspeptin 234 over 30 min through a microdialysis probe located in the stalk-median eminence region |
Applications |
Kisspeptin 234 was shown to reduce pulsatile GnRH secretion in female pubertal monkeys, which supports a key role of kisspeptin in puberty onset. |
Note |
The technical data provided above is for reference only. |
References: 1. Roseweir AK, Kauffman AS, Smith JT, et al. Discovery of potent kisspeptin antagonists delineate physiological mechanisms of gonadotropin regulation. Journal of Neuroscience, 2009, 29(12): 3920-3929. |
质量控制和MSDS
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