97久久久精品综合88久久_亚洲国产精品一_久热热国产久热_97操操操_北条麻妃在线免费观看_精品国自产拍天天拍

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯系我們
丰满少妇AV无码区,大黄网站免费在线观看,成年人免费观看的视频
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-DGUOK/RBITC Conjugated antibody (bs-14277R-RBITC)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-14277R-RBITC
英文名稱 Rabbit Anti-DGUOK/RBITC Conjugated antibody
中文名稱 羅丹明(RBITC)標記的脫氧鳥苷激酶抗體
別    名 Deoxyguanosine kinase mitochondrial; dGK; Deoxyguanosine kinase; DGUOK; DGUOK_HUMAN; Deoxyguanosine kinase, mitochondrial.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 免疫學  神經生物學  激酶和磷酸酶  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Cow, Horse, Rabbit, Sheep, )
產品應用 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 28kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human DGUOK
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 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.
產品介紹 background:
In mammalian cells, the phosphorylation of purine deoxyribonucleosides is mediated predominantly by two deoxyribonucleoside kinases, cytosolic deoxycytidine kinase and mitochondrial deoxyguanosine kinase. The protein encoded by this gene is responsible for phosphorylation of purine deoxyribonucleosides in the mitochondrial matrix. In addition, this protein phosphorylates several purine deoxyribonucleoside analogs used in the treatment of lymphoproliferative disorders, and this phosphorylation is critical for the effectiveness of the analogs. Alternative splice variants encoding different protein isoforms have been described for this gene. [provided by RefSeq, Jul 2008]

Function:
Mitochondrial deoxyguanosine kinase (DGUOK) is required for the phosphorylation of several deoxyribonucleosides and certain purine deoxykribonucleoside analogs widely employed as antiviral and chemotherapeutic agents. Purine deoxyribonucleoside analogs are extensively used in treatment of lymphoproliferative disorders. These compounds are administered as pro-drugs, and their efficiency is dependent on intracellular phosphorylation to the corresponding triphosphates. In mammalian cells, the phosphorylation of purine deoxyribonucleosides is mediated predominantly by 2 deoxyribonucleoside kinases: cytosolic deoxycytidine kinase (DCK) and mitochondrial deoxyguanosine kinase (DGUOK also known as DGK). DGUOK expression is ubiquitous, with highest levels in muscle, brain, liver and lymphoid tissues. Defects in DGUOK are a cause of mitochondrial DNA depletion syndrome (MDS). MDS is a clinically heterogeneous group of disorders characterized by a reduction in mitochondrial DNA (mtDNA) copy number. Primary mtDNA depletion is inherited as an autosomal recessive trait and may affect single organs, typically muscle or liver, or multiple tissues. Mitochondrial DNA depletion syndromes are phenotypically heterogeneous, autosomal recessive disorders characterized by tissue-specific reduction in mtDNA copy number. Affected individuals with the hepatocerebral form of mtDNA depletion syndrome have early progressive liver failure and neurologic abnormalities, hypoglycemia, and increased lactate in body fluids.

Subunit:
Homodimer.

Subcellular Location:
Mitochondrion.

Tissue Specificity:
Ubiquitous. Highest expression in muscle, brain, liver and lymphoid tissues.

DISEASE:
Mitochondrial DNA depletion syndrome 3 (MTDPS3) [MIM:251880]: A disorder due to mitochondrial dysfunction characterized by onset in infancy of progressive liver failure, hypoglycemia, increased lactate in body fluids, and neurologic abnormalities including hypotonia, encephalopathy, peripheral neuropathy. Affected tissues show both decreased activity of the mtDNA-encoded respiratory chain complexes and mtDNA depletion. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the DCK/DGK family.

Database links:

Entrez Gene: 1716 Human

Entrez Gene: 27369 Mouse

Omim: 601465 Human

SwissProt: Q16854 Human

SwissProt: Q4ZG09 Human

SwissProt: Q7L1W9 Human

SwissProt: Q9BVK7 Human

SwissProt: Q3TKB4 Mouse

SwissProt: Q504N4 Mouse

SwissProt: Q8CBU2 Mouse

SwissProt: Q91XI5 Mouse

SwissProt: Q9QX60 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.kastlife.cn 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
主站蜘蛛池模板: 天天躁日日躁狠狠躁2021a1 | 在线不卡AV片免费观看 | 国产精品久久久久久久久大全 | 成人片黄网站色大片免费毛片 | 国产区精品一区二区不卡中文 | 日韩三级.com| 免费国产黄线在线播放 | 人牛交VIDE欧美XXXX | 国产成年无码久久久免费 | 美国一级大黄一片免费中文 | 国产午夜精华液 | 超91在线 | 成年日韩片AV在线网站医生 | 久久精品水蜜桃AV综合天堂 | 亚洲精品在线观看视频 | 冈江凛性色精品一区二区 | 国产视频手机在线观看 | 少妇人妻偷人精品无码视频 | 国产福利在线观看91精品 | 日本xxxx裸体xxxx野外 | 无码AV波多野结衣久久 | 草草网站 | 久久免费在线观看视频 | 波多野结衣中文字幕免费观看 | 国产精品久久久久久久久绿色 | 4438成人网 | 国产AV无码专区亚洲精品 | 制服丝袜自拍另类第1页 | 欧美激情片一区二区 | 麻豆久久久久久久 | 成年人在线免费看的惊悚动作片 | 中文字幕在线观看不卡视频 | 欧美日韩免费观看视频 | 二三区日韩 | 影音先锋亚洲AV少妇熟女 | 免费无码国产V片在线观看 久久久激情网 | 国产99视频精品免费观看6 | 37人体做爰久久久久久 | 国产女教师一爽a片 | 亚洲精一区二区三区 | 中文字幕欧美日韩一区 |