TMEM270抗体TMEM270兔多抗抗体Williams-
Beuren syndrome chromosomal region 28 protein抗体TMEM270 Antibody, FITC conjugated抗体- ￥880 - 1320
- CUSABIO
- CN
- CSB-PA744250LC01HU
- 2025年07月13日
- /
- Rabbit
- Human
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Recombinant Human Transmembrane protein 270 protein (206-265AA)
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Upon receipt, store at -20℃ or -80℃. Avoid repeated freeze.
- 克隆性：
Polyclonal
- 标记物：
FITC
- 适应物种：
Human
- 保质期：
6个月
- 抗原来源：
Homo sapiens (Human)
- 目录编号：
Q6UE05
- 级别：
优
- 库存：
200
- 供应商：
武汉华美生物工程有限公司
- 宿主：
Rabbit
- 应用范围：
/
- 浓度：
>95%,Protein G purified
- 靶点：
TMEM270
- 抗体英文名：
TMEM270 Antibody, FITC conjugated
- 抗体名：
TMEM270;WBSCR28;Transmembrane protein 270;Williams-Beuren syndrome chromosomal region 28 protein
- 规格：
100μg/50μg
| 规格： | 100μg | 产品价格： | ￥1320.0 |
|---|---|---|---|
| 规格： | 50μg | 产品价格： | ￥880.0 |
保存缓冲液
Preservative: 0.03% Proclin 300Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
功能
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文献和实验Molecular and Genetic Aspects of DiGeorge/Velocardiofacial Syndrome
Cytogenetic, molecular, and clinical genetic studies have contributed to our understanding of the etiology, pathogenesis, and natural history of DiGeorge syndrome (DGS) and velocardiofacial syndrome (VCFS). Submicroscopic deletions
Williams-Beuren Syndrome Diagnosis Using Fluorescence In Situ Hybridization
Williams-Beuren syndrome (WBS) is most commonly caused by a 1.5-Mb hemizygous deletion of chromosome 7q11.23. Other genomic rearrangements of this region have also been described, some as polymorphisms and others as rare variants
breakpoint in FIP1L1 and the telomeric breakpoint in PDGFRA . The breakpoints in FIP1L1 are diverse (introns 7 to 10), but the breakpoints in PDGFRA are always in exon 12 (encoding the juxtamembrane region). because the chromosomal deletion is only 800 kb
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