11034731001
Roche
引物“随机”
lyophilized, sufficient for ≤400 reactions, pkg of 2 mg (Primer, Random pd(N)6 Potassium Salt)
别名:
引物
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10 G
CN¥2,079.15
50 G
CN¥8,202.21
250 G
CN¥27,811.75
CN¥2,079.15
国内现货，预计发货时间April 27, 2025详情
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10 G
CN¥2,079.15
50 G
CN¥8,202.21
250 G
CN¥27,811.75
About This Item
UNSPSC代码:
41106300
CN¥2,079.15
国内现货，预计发货时间April 27, 2025详情
推荐产品
表单
lyophilized
质量水平
用途
sufficient for ≤400 reactions
包装
pkg of 2 mg (Primer, Random pd(N)6 Potassium Salt)
制造商/商品名称
Roche
储存温度
−20°C
1 of 4
此商品 | 74884 | 74885 | 51832 |
|---|---|---|---|
| assay ≥99.0% (T) | assay ≥99.0% (T) | assay ≥97.0% (T) | assay ≥99.0% (T) |
| form sheet | form sheet | form sheet | form solid |
| suitability corresponds to standard for RP gradient test, corresponds to standard for filter test | suitability - | suitability - | suitability corresponds to standard for RP gradient test, corresponds to standard for filter test |
| technique(s) ion pair chromatography: suitable | technique(s) ion pair chromatography: suitable | technique(s) - | technique(s) ion pair chromatography: suitable |
| mol wt 234.29 g/mol | mol wt 234.29 g/mol | mol wt - | mol wt 220.26 g/mol |
| mp ≥300 °C (lit.) | mp ≥300 °C (lit.) | mp ≥300 °C (lit.) | mp - |
储存分类代码
12 - Non Combustible Liquids
WGK
nwg
闪点(°F)
does not flash
闪点(°C)
does not flash
法规信息
常规特殊物品
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Nucleic acids research, 44(5), 2393-2408 (2016-01-29)
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Monika Hiller et al.
PloS one, 13(10), e0204485-e0204485 (2018-10-03)
Duchenne muscular dystrophy is a lethal disease caused by lack of dystrophin. Skipping of exons adjacent to out-of-frame deletions has proven to restore dystrophin expression in Duchenne patients. Exon 51 has been the most studied target in both preclinical and
Vadim Alexandrov et al.
Nature biotechnology, 34(8), 838-844 (2016-07-05)
Rapid technological advances for the frequent monitoring of health parameters have raised the intriguing possibility that an individual's genotype could be predicted from phenotypic data alone. Here we used a machine learning approach to analyze the phenotypic effects of polymorphic
Vittoria Pagliarini et al.
Journal of neurochemistry, 153(2), 264-275 (2019-12-08)
Spinal muscular atrophy (SMA) is a motor neuron disease caused by loss of function mutations in the Survival Motor Neuron 1 (SMN1) gene and reduced expression of the SMN protein, leading to spinal motor neuron death, muscle weakness and atrophy.
Piergiorgio La Rosa et al.
Journal of neurochemistry, 157(4), 1153-1166 (2020-09-23)
Neural Progenitor Cells (NPCs) are multipotent cells that are able to self-renew and differentiate into neurons. The size of the initial pool of NPCs during the brain development strongly affects the number of neurons that compose cortical multi-layer during development.
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