UBAP1抗体UBAP1一抗抗体Nasopharyngeal
carcinoma-associated gene 20 protein antibody抗体UBAP1 Antibody抗体- ￥1100 - 1980
- CUSABIO
- CN
- CSB-PA955770
- 2025年07月10日
- ELISA,IHC;ELISA:1:2000-1:5000,IHC:1:25-1:100
- Rabbit
- Human,Mouse,Rat
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Fusion protein of Human UBAP1
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Upon receipt, store at -20℃ or -80℃. Avoid repeated freeze.
- 克隆性：
/
- 标记物：
Non-conjugated
- 适应物种：
Human,Mouse,Rat
- 保质期：
6个月
- 抗原来源：
Homo sapiens (Human)
- 目录编号：
Q9NZ09
- 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：
ELISA,IHC;ELISA:1:2000-1:5000,IHC:1:25-1:100
- 浓度：
>95%,Antigen affinity purification
- 靶点：
UBAP1
- 抗体英文名：
UBAP1 Antibody
- 抗体名：
UBAP1 antibody;NAG20 antibody;Ubiquitin-associated protein 1 antibody;UBAP-1 antibody;Nasopharyngeal carcinoma-associated gene 20 protein antibody
- 规格：
100μl/50μl
| 规格： | 100μl | 产品价格： | ￥1980.0 |
|---|---|---|---|
| 规格： | 50μl | 产品价格： | ￥1100.0 |
保存缓冲液
-20℃, pH7.4 PBS, 0.05% NaN3, 40% Glycerol功能
This gene is a member of the UBA domain family, whose members include proteins having connections to ubiquitin and the ubiquitination pathway. The ubiquitin associated domain is thought to be a non-covalent ubiquitin binding domain consisting of a compact three helix bundle. This particular protein originates from a gene locus in a refined region on chromosome 9 undergoing loss of heterozygosity in nasopharyngeal carcinoma (NPC). Taking into account its cytogenetic location, this UBA domain family member is being studies as a putative target for mutation in nasopharyngeal carcinomas. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验-binding protein α-1 subunit (GNAZ ), carbamyl phosphate synthetase I (CPS I ), insulin-like growth factor (IGF)-II, and 10 ribosomal proteins genes. Eighteen genes were downregulated including acute phase genes, a novel gene, and particularly
Mutation of p53 Tumor Suppressor Gene in Hepatocellular Carcinoma
In recent years, the most commonly observed genetic alteration in hepatocellular carcinoma (HCC), as in many other tumors affecting man, has been reported to be the mutation of the p53 coding gene (1 ,2 ). This gene has the features
Detection of Risks Associated with Coat Protein Transgenics
considerable attention and has been reviewed several times previously (see refs. 1 –16 ). The viral genes most frequently used to provide protection are those for the coat protein (CP), the viral replicase, and the cell-to-cell movement protein (see reviews
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