推荐产品
等級
certified reference material
品質等級
形狀
liquid
特點
(Snap-N-Spike®)
包裝
ampule of 1 mL
製造商／商標名
Cerilliant®
濃度
5 μg/mL in ethanol
mp
-143.99 °C
應用
clinical testing
clinical testing
格式
single component solution
儲存溫度
−70°C
SMILES 字串
O[C@@H](C[C@H](O)C/1=C)CC1=C\C=C2[C@@](CC[C@]3([H])[C@H](C)CCC[13C](O)([13CH3])[13CH3])([H])[C@]3(C)CCC\2
InChI
1S/C27H44O3/c1-18(8-6-14-26(3,4)30)23-12-13-24-20(9-7-15-27(23,24)5)10-11-21-16-22(28)17-25(29)19(21)2/h10-11,18,22-25,28-30H,2,6-9,12-17H2,1,3-5H3/b20-10+,21-11-/t18-,22-,23-,24+,25+,27-/m1/s1/i3+1,4+1,26+1
InChI 密鑰
GMRQFYUYWCNGIN-SYUIRNBGSA-N
一般說明
一种稳定标记的内部标准，适用于LC-MS/MS测定1,25-二羟基维生素D3水平。1,25-二羟基维生素D3，也称为骨化三醇，是维生素D的激素活性代谢物，负责调节钙。1,25-二羟基维生素D3的测定用于区分原发性甲状旁腺功能亢进和癌症高钙血症，并用于鉴别维生素D依赖型佝偻病。
應用
- Leigh Syndrome with HIBCH Mutations: Discusses the metabolic effects of mutations related to Leigh syndrome and includes information on 3-hydroxybutyryl carnitine isomers (Wang et al., 2021, frontiersin.org).
- Highly Efficient Ketone Body Treatment in Leukodystrophy: Highlights the therapeutic potential of L-carnitine in treatments, specifically focusing on the metabolism of L-3-hydroxybutyryl-CoA in the context of fatty acid β-oxidation disorders (Gautschi et al., 2015, nature.com).
其他說明
法律資訊
CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany
訊號詞
Danger
危險聲明
危險分類
Eye Irrit. 2 - Flam. Liq. 2
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 1
閃點（°F）
57.2 °F - closed cup
閃點（°C）
14.0 °C - closed cup
其他客户在看
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Niemann-Pick type C (NPC) disease is a multisystem disorder caused primarily by a mutation in the npc1 gene. These studies evaluated the effect of genetic background, deletion of additional genes, and administration of several agents on the age at death
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Central amygdala (CeA) neurons that produce corticotropin-releasing factor (CRF) regulate anxiety and fear learning. These CeACRF neurons release GABA and several neuropeptides predicted to play important yet opposing roles in these behaviors. We dissected the relative roles of GABA, CRF
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JCI insight, 2(3), e91103-e91103 (2017-02-15)
Heterozygous germline gain-of-function mutations of G-protein subunit α11 (Gα11), a signaling partner for the calcium-sensing receptor (CaSR), result in autosomal dominant hypocalcemia type 2 (ADH2). ADH2 may cause symptomatic hypocalcemia with low circulating parathyroid hormone (PTH) concentrations. Effective therapies for
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