吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

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  人才招聘  關于我們  聯系我們
狠狠色综合7777久夜色撩人,,国内老熟妇对白XXXXHD,日韩精品久久久久久久电影蜜臀
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Adenylate kinase 2/Cy5 Conjugated antibody (bs-6875R-Cy5)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-6875R-Cy5
英文名稱1 Rabbit Anti-Adenylate kinase 2/Cy5 Conjugated antibody
中文名稱 Cy5標記的腺苷酸激酶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)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  信號轉導  轉錄調節(jié)因子  激酶和磷酸酶  線粒體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Sheep, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 26kDa
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 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:
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.
版權所有 2004-2026 www.xucheq.com 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(yī)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
久久午夜夜伦鲁鲁片无码免费| 色哟哟网站入口在线观看视频| 无码一区二区三区在线| 欧美乱大交XXXXX| 被公牛日到了高潮| 99精品亚洲AV无码国产另类| 久久99精品久久久久久| 亚洲精品无码久久久久久久| 国产成人一区二区三区影| 少妇荡乳情欲办公室456视频| 粉嫩av国产一区二区三区| 亚洲中文字幕无码AV| 中文字幕人妻色偷偷久久| 国产乡下妇女做爰| 欧美性大战XXXXX久久久| 欲求不満の人妻松下纱荣子| 色欲AV永久无码精品无码蜜桃| 性色AV无码不卡中文字幕| AV鲁丝一区鲁丝二区鲁丝三区| 人妻无码第一区二区三区| 少妇被躁爽到高潮无码人狍大战| 国产A级三级三级三级| 欧美激情一区二区三区在线| 国产亚洲精品久久久久久禁果TV| 肥嫩多毛的大荫户| 精品亚洲麻豆1区2区3区| 国产男女猛烈无遮挡免费视频网站| 国产精品99精品无码视亚| 久久人人爽天天玩人人妻精品| 亚洲色欲一区二区三区在线观看| 日本一区二区三区视频| 丰满雪白人妻人爽AV精品| 欧美人妻一区二区三区| 国产产无码乱码精品久久鸭 | 无码高潮又爽又黄又刺激视频| 免费看又黄又无码的网站| av无码在线| 亚洲最大成人网站| 极品少妇XXXX精品少妇偷拍| 男人的天堂AV网站| 18禁男女爽爽爽午夜网站免费|