FITC标记的17号染色体开放阅读框42抗体

¥2980
LMAI Bio
中国/美国/欧洲
2022-03-24 18:07

上海联迈生物工程有限公司

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上海联迈生物工程有限公司
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产品属性
供应商上海联迈生物工程有限公司
数量大量
靶点详见说明书
级别1
目录编号LM-9639R-FITC
克隆性多克隆
抗原来源Rabbit
保质期1年
抗体英文名Anti-C17orf42/FITC
抗体名Anti-C17orf42/FITC
标记物FITC标记
宿主Human, Mouse, Rat, Dog, Pig,
适应物种Human, Mouse, Rat, Dog, Pig,
免疫原详见说明书
亚型IGg
形态粉末、液体、冻干粉
应用范围ICC=1:50-200 IF=1:50-200
浓度1mg/ml
保存条件-20 °C
规格100ul
产品说明
FITC标记的17号染色体开放阅读框42抗体
英文名称Anti-C17orf42/FITC
中文名称FITC标记的17号染色体开放阅读框42抗体
别 名Chromosome 17 open reading frame 42; FLJ22729; Hypothetical protein LOC79736; MGC24674; UPF0629 protein C17orf42; TEFM_HUMAN.
规格价格100ul/2980元 购买 大包装/询价
说 明 书100ul
研究领域肿瘤 免疫学 信号转导 表观遗传学
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human, Mouse, Rat, Dog, Pig,
产品应用ICC=1:50-200 IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量38kDa
性 状Lyophilized or Liquid
浓 度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human C17orf42
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.
产品介绍background:
C17orf42 is a 360 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene mapping to human chromosome 17. Chromosome 17 makes up over 2.5% of the human genome with about 81 million bases encoding over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1. Tumor suppressor p53 is necessary for maintenance of cellular genetic integrity by moderating cell fate through DNA repair versus cell death. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Like p53, BRCA1 is directly involved in DNA repair, specifically it is recognized as a genetic determinant of early onset breast cancer and predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes. Chromosome 17 is also linked to neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.

Function:
Transcription elongation factor which increases mitochondrial RNA polymerase processivity. Regulates transcription of the mitochondrial genome, including genes important for the oxidative phosphorylation machinery. [SUBUNIT] Interacts with POLRMT. 

Subcellular Location:
Mitochondrion matrix. Mitochondrion matrix, mitochondrion nucleoid. 

Similarity:
Belongs to the TEFM family. 

Database links:

Entrez Gene: 124944 Human

SwissProt: Q8IXM2 Human

Unigene: 511801 Human



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