相关产品推荐更多 >

Human CLMN shRNA Plasmid/Human CLMN shRNA Plasmid/Human CLMN shRNA Plasmid
询价
PES Syringe Filters, 0.45 um, 25mm/PES Syringe Filters, 0.45 um, 25mm/PES Syringe Filters, 0.45 um, 25mm
询价
ANAPC13 siRNA/ANAPC13 siRNA/ANAPC13 siRNA
询价
【干冰】Ether C18 Lysobisphosphatidic acid/【干冰】Ether C18 Lysobisphosphatidic acid
询价
Human ZNF100 shRNA Plasmid/Human ZNF100 shRNA Plasmid/Human ZNF100 shRNA Plasmid
询价
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
储存于-20 ° C
- 保质期:
1年
- 英文名:
Hydrocortisone 21-hemisuccinate (sodium salt)
- 库存:
100
- 供应商:
艾美捷科技
- CAS号:
无
- 规格:
100mg
Hydrocortisone 21-hemisuccinate (sodium salt),Hydrocortisone 21-hemisuccinate (sodium salt),Hydrocortisone 21-hemisuccinate (sodium salt),Hydrocortisone 21-hemisuccinate (sodium salt)
Hydrocortisone 21-hemisuccinate (sodium salt)-Hydrocortisone 21-hemisuccinate (sodium salt)
产品货号:APE-C3154-100
产品规格:100mg
该Hydrocortisone 21-hemisuccinate (sodium salt)产品的背景资料具体查看产品。

该Hydrocortisone 21-hemisuccinate (sodium salt)产品的产品描述具体查看产品。

Hydrocortisone 21-hemisuccinate (sodium salt)-Hydrocortisone 21-hemisuccinate (sodium salt)储存于-20 ° C
点击:Hydrocortisone 21-hemisuccinate (sodium salt)-Hydrocortisone 21-hemisuccinate (sodium salt)查看更详细产品说明,更多应用、储存、价格、货期等信息请垂询艾美捷科技有限公司。更多APExBIO公司特色小分子抑制剂等产品评论,请点击查看艾美捷特色产品中心。
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验virus and breakdown products of complement component C3 Forms a signaling complex with CD19, CD81 and CD225 Both CD21 and CD23 are dendritic cell markers Hodgkin’s lymphoma demonstrates disruption of follicular dendritic cell-germinal
, together with other proteases and an aminopeptidase, during stationary phase when the fungus is grown by submerged culture. The enzyme is so named because the organism can grow on native keratin as sole carbohydrate and nitrogen source owing to the enzyme’s ability to digest
Characterization of Gene Rearrangements and Gene Conversion Events in the 21-Hydroxylase Gene
Congenital adrenal hyperplasia (CAH) is an inherited disorder of steroidogenesis with a wide spectrum of expression. In about 95% of cases, the disease is the result of 21-hydroxylase deficiency, an autosomal recessive condition that maps
技术资料暂无技术资料 索取技术资料






