注意事项:书纯度高,检测/鉴别精确,稳定性强,为了防止产品含量降低,不宜暴露在空气中,应防潮、避光和抗氧化包装,保存应以提高物质稳定性为原则,尽可能在干燥、低温条件下储藏(液体或易潮解物质分装在熔封的玻璃安瓶内)。
不能直接用于人体,出库的产品全部经过严格的检测,保证质量。标准品/对照品一般用于鉴别、检查和含量 (或效价)测定。对于鉴别来说,只要确认未混淆标准物质 即可,而检查和含量测定则不同,大部分检查项目和含量测定项目均有明确的标准。这就要求在进行检验时要控制实验误差,在进行标准物质称量时未严格按照药典等标准要求进行。
汉黄芩苷;Wogo
noside CAS: 51059-44-0 规格: 20mg
黄芩素;Baicalein CAS: 491-67-8 规格: 20mg
黄豆黄苷; Glycitin CAS: 40246-10-4 规格: 20mg
黄芩苷;Baicalin CAS: 21967-41-9 规格: 20mg
β-胡萝卜素;β-Carotene CAS: 7235-40-7 规格: 100mg
胡椒碱;Piperine CAS: 94-62-2 规格: 20mg
高熊果酚苷; CAS: 25712-94-1 规格: 10mg
甘草次酸十八酯;Stearyl glyc CAS: 13832-70-7 规格: 20mg
甘草酸二钾;Dipotassium gl CAS: 68797-35-3 规格: 20mg
戈米辛J;Gomisin J CAS: 66280-25-9 规格: 10mg
瓜氨酸;L(+)-Citrulline CAS: 372-75-8 规格: 20mg
根薯酮内酯B;Taccalo
nolide CAS: 108885-69-4 规格: 20mg
根薯酮内酯A;Taccalo
nolide CAS: 108885-68-3 规格: 20mg
D-果糖;D(-)-Fructose CAS: 57-48-7 规格: 100mg
广藿香酮;Pogostone CAS: 规格: 20mg
PP40 is the predominant form of cerebrovascular amyloid. Amyloid is not found outside the nervous system. The principal clinical characteristics are recurrent cerebral and cerebellar hemorrhages, recurrent strokes, cerebral ischemia, cerebral infarction, and progressive mental deterioration. onset of the disease is in middle age (44 to 60 years). Patients develop cerebral hemorrhage because of the severe cerebral amyloid angiopathy. Parenchymal amyloid deposits are rare and largely in the form of pre-amyloid lesions or diffuse plaque-like structures. They are Congo red negative and lack the dense amyloid cores commonly present in Alzheimer disease.
Defects in APP are the cause of amyloidosis cerebroarterial Italian type (AMYLCAIT) [MIM:605714]. AMYLCAIT is a hereditary localized amyloidosis due to amyloid-beta A4 peptide(s) deposition in the cerebral vessels, resulting in cerebral amyloid angiopathy. Amyloid is not found outside the nervous system. It is a condition very similar to AMYLCAD, but the clinical course is less severe. Patients manifest mild cognitive decline, recurrent strokes, and epilepsy in some cases. There are extensive amyloid deposits in leptomeningeal and cortical vessels and, to a lesser extent, in the neuropil of the cerebral cortex, in the absence of neurofibrillary tangles.
Defects in APP are the cause of amyloidosis cerebroarterial Iowa type (AMYLCAIW) [MIM:605714]. AMYLCAIW is a hereditary amyloidosis due to amyloid-beta A4 peptide(s) deposition. Patients have progressive aphasic dementia, leukoencephalopathy, and occipital calcifications.
Similarity : Belongs to the APP family.
Contains 1 BPTI/Kunitz inhibitor domain.
Database links : UniProtKB/Swiss-Prot: P05067.3
Entrez Gene: 351 Human
Entrez Gene: 11820 Mouse
Entrez Gene: 54226 Rat
Omim: 104760 Human
英文名称 Anti-ARIP2a
中文名称 激活素受体2A抗体
别 名 Activin receptor 2A; Activin receptor type 2A; ACTR 2; ACTR IIA; ACTR2; ActRIIa; Acvr 2; Acvr 2A; Acvr2; Acvr2a; OTTHUMP00000197918.
苦玄参苷IA 97230-47-2使用说明书浓 度 1mg/1ml
规 格 0.2ml/200μg
抗体来源 Rabbit
克隆类型 polyclonal
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