亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

掃碼關(guān)注公眾號(hào)           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  關(guān)于我們  聯(lián)系我們
四虎影视久久久免费,男人扒开女人下面狂躁动漫版,18禁男女爽爽爽午夜网站免费
Rabbit Anti-Adenylate kinase 2/FITC Conjugated antibody (bs-6875R-FITC)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@www.chomd.com.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@www.chomd.com.cn
說(shuō) 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-6875R-FITC
英文名稱 Rabbit Anti-Adenylate kinase 2/FITC Conjugated antibody
中文名稱 FITC標(biāo)記的腺苷酸激酶2抗體
別    名 mitochondrial; Adenylate kinase 2; Adenylate kinase isoenzyme 2; ADK2; AK 2; ak2; ATP AMP transphosphorylase; ATP AMP transphosphorylase; ATP-AMP transphosphorylase 2; EC 2.7.4.3; KAD2_HUMAN.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買        大包裝/詢價(jià)
說(shuō) 明 書 100ul  
研究領(lǐng)域 細(xì)胞生物  信號(hào)轉(zhuǎn)導(dǎo)  轉(zhuǎn)錄調(diào)節(jié)因子  激酶和磷酸酶  線粒體  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Sheep, )
產(chǎn)品應(yīng)用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 26kDa
細(xì)胞定位 細(xì)胞膜 線粒體
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Adenylate kinase 2/AK2
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 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(chǎn)品介紹 background:
Adenylate kinases are involved in regulating the adenine nucleotide composition within a cell by catalyzing the reversible transfer of phosphate groups among adenine nucleotides. Three isozymes of adenylate kinase, namely 1, 2, and 3, have been identified in vertebrates; this gene encodes isozyme 2. Expression of these isozymes is tissue-specific and developmentally regulated. Isozyme 2 is localized in the mitochondrial intermembrane space and may play a role in apoptosis. Mutations in this gene are the cause of reticular dysgenesis. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 1 and 2.[provided by RefSeq, Nov 2010]

Function:
Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. This small ubiquitous enzyme involved in energy metabolism and nucleotide synthesis that is essential for maintenance and cell growth. Plays a key role in hematopoiesis.

Subunit:
Monomer.

Subcellular Location:
Mitochondrion intermembrane space.

Tissue Specificity:
Present in most tissues. Present at high level in heart, liver and kidney, and at low level in brain, skeletal muscle and skin. Present in thrombocytes but not in erythrocytes, which lack mitochondria. Present in all nucleated cell populations from blood, while AK1 is mostly absent. In spleen and lymph nodes, mononuclear cells lack AK1, whereas AK2 is readily detectable. These results indicate that leukocytes may be susceptible to defects caused by the lack of AK2, as they do not express AK1 in sufficient amounts to compensate for the AK2 functional deficits (at protein level).

DISEASE:
Defects in AK2 are the cause of reticular dysgenesis (RDYS) [MIM:267500]; also known as aleukocytosis. RDYS is the most severe form of inborn severe combined immunodeficiencies (SCID) and is characterized by absence of granulocytes and almost complete deficiency of lymphocytes in peripheral blood, hypoplasia of the thymus and secondary lymphoid organs, and lack of innate and adaptive humoral and cellular immune functions, leading to fatal septicemia within days after birth. In bone marrow of individuals with reticular dysgenesis, myeloid differentiation is blocked at the promyelocytic stage, whereas erythro- and megakaryocytic maturation is generally normal.In addition, affected newborns have bilateral sensorineural deafness. Defects may be due to its absence in leukocytes and inner ear, in which its absence can not be compensated by AK1.

Similarity:
Belongs to the adenylate kinase family. AK2 subfamily.

Database links:

Entrez Gene: 204 Human

Entrez Gene: 11637 Mouse

Entrez Gene: 24184 Rat

Omim: 103020 Human

SwissProt: P54819 Human

SwissProt: Q9WTP6 Mouse

SwissProt: P29410 Rat

Unigene: 470907 Human

Unigene: 29460 Mouse

Unigene: 3421 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.www.chomd.com.cn 北京博奧森生物技術(shù)有限公司
通過(guò)國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號(hào): 00124Q34771R2M/1100
通過(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
主站蜘蛛池模板: 久热这里只有精品免费精品| 精品久久久久中文字幕人妻蜜臀97资源 | 国产精品久久久久久无码专区男友| 欧美精品一在线发布| 日本精品国产毛片A片18区| 丝袜亚洲AV中文| 人妻中文字幕久久中文| 国产草莓视频在线观看免费|国产 国产超碰人人做人人爱,最新亚洲AV日韩AV二 | 精品国产黑色丝袜高跟鞋h | 亚洲精品无码久久毛片18特黄老色枇 | 亚洲Av秘?无码一区二区| 亚洲精品无码成人片久久不卡浪 | 亚洲国产一二三精品无码不卡 站长工具| 亚洲一区二区三区丝袜AV| 亚洲国产一二三精品无码不卡 站长工具 | 91视频91最新久久久久久久| 7777精品久久久大香线蕉,精品国产一区| 国产成人精品福利网站APP| 亚洲中文字幕精品久久久久久精品久 | 国产综合成人久久大片91|亚洲国产| 久久艾草毛片一级| 国产v片在线观看v| 亚洲国产欧洲综合997久久_久久九九国产 | 严洲产国偷V产偷V自拍性色AV| 亚洲综合区小说区激情区,亚洲综合色| 人人超碰欧美一本二本 | 精品国产污污免费网站东 | 久久久久亚洲精品天堂免费软件下载 | 在线看片毛片无码永久免费监控摄像| 一级毛片免费全部播放完整剧情为| 里番人妻过夜1—2集| 国产又黄又爽又猛免费视频电影 | 91在线无码精品秘?入口91| 欧亚精品卡一卡二卡三优惠| 自拍视频在线观看一区二区3区 | 国产99视频精品免视看67| 婷婷五月中文在线视频| 成年网在线观看免费观看网址 | 亚洲欧美日韩中文字幕视频屏幕| 色丝袜AV区| 国产无遮挡又爽又大又粗扩肛|