FITC标记的FAM172A蛋白抗体-抗体-抗体-生物在线
FITC标记的FAM172A蛋白抗体

FITC标记的FAM172A蛋白抗体

商家询价

产品名称: FITC标记的FAM172A蛋白抗体

英文名称: Anti-FAM172A/FITC

产品编号: HZ-13772R-FITC

产品价格: null

产品产地: 中国/上海

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: ICC=1:50-200 IF=1:50-200

上海沪震实业有限公司
  • 联系人 : 鲍丽雯
  • 地址 : 上海市闵行区闵北路88弄1-30号第22幢AQ136室
  • 邮编 : 200612
  • 所在区域 : 上海
  • 电话 : 139****0749
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  • 邮箱 : www.shzbio.net

 Rabbit Anti-FAM172A/FITC Conjugated antibody

FITC标记的FAM172A蛋白抗体

 

英文名称 Anti-FAM172A/FITC
中文名称 FITC标记的FAM172A蛋白抗体
别    名 C5orf21; F172A_HUMAN; fam172a; Family with sequence similarity 172, member A; Protein FAM172A  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 肿瘤  细胞生物  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Rabbit, 
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 131kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human FAM172A
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:
FAM172A is a 416 amino acid secreted protein belonging to the UPF0528 family and is encoded by a gene located on human chromosome 5. Chromosome 5 contains 181 million base pairs and comprises nearly 6% of the human genome. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5-associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

Subcellular Location:
Secreted.

Similarity:
Belongs to the UPF0528 family.

Database links:

Entrez Gene: 83989 Human

Entrez Gene: 68675 Mouse

Entrez Gene: 294606 Rat

SwissProt: Q8WUF8 Human

SwissProt: Q3TNH5 Mouse

Unigene: 600086 Human

Unigene: 343005 Mouse

Unigene: 203242 Rat



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

FAM172A是属于UPF0528家族的416个氨基酸分泌蛋白,由位于人类5号染色体上的基因编码。第5染色体包含1亿8100万个碱基对,并包含人类基因组的近6%。5号染色体通过ERCC8基因与Cockayne综合征相关,家族性腺瘤性息肉病通过APC抑癌基因与腺瘤性息肉病相关。Treacher Collins综合征也是5号染色体相关的,是由TCOF1基因内的插入或缺失引起的。5号染色体p臂缺失导致Cri du chat综合征,而q臂或5号染色体缺失在治疗相关的急性髓细胞白血病和骨髓增生异常综合征中很常见。