- ￥11900
- Metasystems
- 德国
- D-0213-120-DI
- 2025年08月31日
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- 详细信息
- 文献和实验
- 技术资料
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- 保质期：
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- 英文名：
XCyte 13, Chromosome 13 mBAND probe
- 库存：
大量
- 供应商：
欣博盛
- 规格：
120 µl
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文献和实验Detection of Chromosome 13 Deletions by Fluorescent In Situ Hybridization
with these diseases, one of which is abnormalities of chromosome 13. Using the two techniques simultaneously (i.e., cIg-FISH), we have demonstrated that approx 50% of patients with MM have abnormalities of chromosome 13, mostly monosomy, and when present involving
Molecular Detection of t(11;14)(q13;q32) in Mantle Cell Lymphoma
Mantle cell lymphoma (MCL) is characterized by the presence of t(11;14)(q13;q32) which juxtaposes CCND-1 gene (also known as BCL-1 , PRAD-1 ) at 11q13 with an enhancer of the IGH@ gene at 14q32. The resultant overexpression of cyclin D1 plays
In situ hybridisation to alpha satellite sequences (chromosome specific)
hybridised to a chromosome 17 specific alpha satellite probe. We buy our probes from Appligene/Oncor although they are very expensive and the telesales staff are rude. Starting material We have two types of starting material; (i) tissue culture
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