FITC标记的5号染色体开放阅读框33抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的5号染色体开放阅读框33抗体

FITC标记的5号染色体开放阅读框33抗体

商家询价

产品名称: FITC标记的5号染色体开放阅读框33抗体

英文名称: Anti-C5ORF33/FITC

产品编号: HZ-9999R-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

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 Rabbit Anti-C5ORF33/FITC Conjugated antibody

FITC标记的5号染色体开放阅读框33抗体

 

产品编号 bs-9999R-FITC
英文名称 Anti-C5ORF33/FITC
中文名称 FITC标记的5号染色体开放阅读框33抗体
别    名 C5orf33; CE033_HUMAN; Chromosome 5 open reading frame 33; NADKD1.  
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  免疫学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Dog, Pig, Rabbit, Zebrafish, Sheep, 
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 43kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human C5ORF33
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:
With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It 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. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf33 gene product has been provisionally designated C5orf33 pending further characterization.

Function:
Mitochondrial NAD(+) kinase that phosphorylates NAD(+) to yield NADP(+). Can use both ATP or inorganic polyphosphate as the phosphoryl donor. Also has weak NADH kinase activity in vitro; however NADH kinase activity is much weaker than the NAD(+) kinase activity and may not be relevant in vivo. 

Subunit:
Homodimer (Probable). 

Subcellular Location:
Mitochondrion.

Tissue Specificity:
Widely expressed.

Similarity:
Belongs to the NAD kinase family. 

Database links:

Entrez Gene: 133686 Human

Entrez Gene: 365699 Rat

SwissProt: Q4G0N4 Human

SwissProt: Q8C5H8 Mouse

SwissProt: Q1HCL7 Rat

Unigene: 81907 Human



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

1亿8100万个碱基对编码约1000个基因,染色体5约为人类基因组DNA的6%。它通过ECRC8基因和家族性腺瘤性息肉病通过腺瘤性息肉病(APC)肿瘤抑制基因与Coojayne综合征相关。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—Douk综合征。在治疗相关的急性髓性白血病和骨髓增生异常综合征中,5q或5号染色体的缺失是常见的。C5ORF33基因产物已暂时指定为C5ORF33,有待进一步鉴定。