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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
常温
- 保质期:
根据瓶身LOT号查询
- 英文名:
Hypotaurine
- 库存:
有现货
- 供应商:
浙江羽翔生物科技有限公司
- CAS号:
300-84-5
- 规格:
10MG
属性
质量水平
200
方案
≥98% (TLC)
颜色
white to off-white
溶解性
H2O: 100 mg/mL
SMILES字符串
NCCS(O)=O
InChI
1S/C2H7NO2S/c3-1-2-6(4)5/h1-3H2,(H,4,5)
InChI key
VVIUBCNYACGLLV-UHFFFAOYSA-N
应用
生化/生理作用
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文献和实验Transcriptomic signature of the follicular somatic compartment surrounding an oocyte with high developmental competence.
During antral folliculogenesis, developmental competence of prospective oocytes is regulated in large part by the follicular somatic component to prepare the oocyte for the final stage of maturation and subsequent embryo development. The underlying molecular mechanisms are poorly understood. Oocytes reaching the advanced stage of follicular growth by administration of exogenous follicle-stimulating hormone (FSH) possess higher developmental competence than oocytes in FSH-untreated smaller follicles. In this study, the transcriptomic profile of the cumulus cells from cows receiving FSH administration (FSH-priming) was compared, as a model of high oocyte competence, with that from untreated donor cows (control). Ingenuity Pathway Analysis showed that cumulus cells receiving FSH-priming were rich in down-regulated transcripts associated with cell movement and migration, including the extracellular matrix-related transcripts, probably preventing the disruption of cell-to-cell contacts. Interestingly, the transcriptomic profile of up-regulated genes in the control group was similar to that of granulosa cells from atretic follicles. Interferon regulatory factor 7 was activated as the key upstream regulator of FSH-priming. Thus, acquisition of developmental competence by oocytes can be ensured by the integrity of cumulus cells involved in cell-to-cell communication and cell survival, which may help achieve enhanced oocyte-somatic cell coupling.
Routine methods for growing the cell lines
extract as usual. Sigma I1882. Make up to 12.5 IU/ml stock solution. Put 10mg in universal, add 0.5ml 0.01N HCl to dissolve. The add 19.5ml D = , mixing on vortex mixer. It will go cloudy, leave it to stand and it will clear. Filter
Routine methods for growing the cell lines
extract as usual. Sigma I1882. Make up to 12.5 IU/ml stock solution. Put 10mg in universal, add 0.5ml 0.01N HCl to dissolve. The add 19.5ml D = , mixing on vortex mixer. It will go cloudy, leave it to stand and it will clear. Filter
,通过预染蛋白marker来确定电泳停止时间。 (4) 湿转法,转膜条件:300mA恒流;0.45um孔径PVDF膜,转膜时间1h。转膜完成后丽春红染色试剂对膜进行染色,观察转膜效果。 (5) 封闭:将膜完全浸没于5%BSA-TBST中,水平摇床孵育2h(RT)。 (6) 一抗孵育:5%BSA-TBST稀释一抗, 4℃水平摇床孵育过夜。 (7) 次日,洗膜:TBST洗3次,每次10min。 (8) 二抗孵育:5%BSA-TBST稀释二抗:山羊抗兔,山羊抗鼠IgG(H+L)HRP
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