Anti-RNF16/TRIM17抗体-抗体-抗体-生物在线
Anti-RNF16/TRIM17抗体

Anti-RNF16/TRIM17抗体

商家询价

产品名称: Anti-RNF16/TRIM17抗体

英文名称: RNF16/TRIM17

产品编号: YB--9161R

产品价格: null

产品产地: 中国/美国

品牌商标: Ybscience

更新时间: 2023-08-17T10:29:50

使用范围: 科研使用

上海钰博生物科技有限公司
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 Anti-RNF16/TRIM17抗体

产品编号 YB-9161R
英文名称 RNF16/TRIM17
中文名称 环指蛋白16抗体
别    名 RBCC; RING finger protein 16; RNF16; TERF; Testis RING finger protein; TRIM 17; Tripartite motif protein 17; TRI17_HUMAN.  
规格价格 100ul/1580元 购买    200ul/2480元 购买    大包装/询价
说 明 书 100ul  200ul
研究领域 细胞生物  信号转导  转录调节因子  表观遗传学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, 
产品应用 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 IF=1:50-200 (石蜡切片需做抗原修复) 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 54kDa
细胞定位 细胞核 细胞浆 
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human TRIM17/RNF16:121-220/477 
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
PubMed PubMed
产品介绍 background:
The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

Function:
May function as an ubiquitin E3 ligase.

Subunit:
Interacts (via coiled coil) with TRIM44 (via coiled coil).

Tissue Specificity:
Almost exclusively in the testis. 

Post-translational modifications:
Auto-ubiquitinated.

Similarity:
Belongs to the TRIM/RBCC family. 
Contains 1 B box-type zinc finger. 
Contains 1 B30.2/SPRY domain. 
Contains 1 RING-type zinc finger.

SWISS:
Q9Y577

Gene ID:
51127

Database links:

Entrez Gene: 51127 Human

Omim: 606123 Human

SwissProt: Q9Y577 Human

Unigene: 121748 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.