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
国产精品v片在线观看不卡,伊人久久大香线蕉av一区,久久a级毛片免费观看
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-ATP6V0A2/Cy5 Conjugated antibody (bs-12761R-Cy5)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-12761R-Cy5
英文名稱1 Rabbit Anti-ATP6V0A2/Cy5 Conjugated antibody
中文名稱 Cy5標記的液泡膜質子轉運ATP酶2型抗體
別    名 a2; A2V ATPase; ARCL; ATP6a2; ATP6N1D; ATP6V0A2; ATPase, H+ transporting, lysosomal V0 subunit a isoform 2; ATPase, H+ transporting, lysosomal V0 subunit a2; Infantile malignant osteopetrosis; J6B7; Lysosomal H(+) transporting ATPase V0 subunit a2; Lysosomal H(+)-transporting ATPase V0 subunit a2; regeneration and tolerance factor; Stv1; TJ6; TJ6M; TJ6s; V ATPase 116 kDa isoform a2; V type proton ATPase 116 kDa subunit a; V type proton ATPase 116 kDa subunit a isoform 2; V-ATPase 116 kDa isoform a2; V-type proton ATPase 116 kDa subunit a isoform 2; Vacuolar proton translocating ATPase 116 kDa subunit a; Vacuolar proton translocating ATPase 116 kDa subunit a isoform 2; Vph1; VPP2_HUMAN; WSS.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  信號轉導  細胞分化  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, 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 98kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ATP6V0A2
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:
The protein encoded by this gene is a subunit of the vacuolar ATPase (v-ATPase), an heteromultimeric enzyme that is present in intracellular vesicles and in the plasma membrane of specialized cells, and which is essential for the acidification of diverse cellular components. V-ATPase is comprised of a membrane peripheral V(1) domain for ATP hydrolysis, and an integral membrane V(0) domain for proton translocation. The subunit encoded by this gene is a component of the V(0) domain. Mutations in this gene are a cause of both cutis laxa type II and wrinkly skin syndrome. [provided by RefSeq, Jul 2009]

Function:
Part of the proton channel of V-ATPases. Essential component of the endosomal pH-sensing machinery. May play a role in maintaining the Golgi functions, such as glycosylation maturation, by controlling the Golgi pH.

Subcellular Location:
Cell membrane. Endosome membrane. In kidney proximal tubules, also detected in subapical vesicles.

Post-translational modifications:
Phosphorylated upon DNA damage, probably by ATM or ATR.

DISEASE:
Defects in ATP6V0A2 are the cause of cutis laxa autosomal recessive type 2A (ARCL2A) [MIM:219200]. An autosomal recessive disorder characterized by an excessive congenital skin wrinkling, a large fontanelle with delayed closure, a typical facial appearance with downslanting palpebral fissures, a general connective tissue weakness, and varying degrees of growth and developmental delay and neurological abnormalities. Some affected individuals develop seizures and mental deterioration later in life, whereas the skin phenotype tends to become milder with age. At the molecular level, an abnormal glycosylation of serum proteins is observed in many cases.
Defects in ATP6V0A2 are a cause of wrinkly skin syndrome (WSS) [MIM:278250]. WSS is rare autosomal recessive disorder characterized by wrinkling of the skin of the dorsum of the hands and feet, an increased number of palmar and plantar creases, wrinkled abdominal skin, multiple musculoskeletal abnormalities, microcephaly, growth failure and developmental delay.

Similarity:
Belongs to the V-ATPase 116 kDa subunit family.

Database links:

Entrez Gene: 338038 Cow

Entrez Gene: 23545 Human

Entrez Gene: 21871 Mouse

Entrez Gene: 116455 Rat

Omim: 611716 Human

SwissProt: O97681 Cow

SwissProt: Q9Y487 Human

SwissProt: P15920 Mouse

Unigene: 25786 Human

Unigene: 1158 Mouse

Unigene: 392098 Mouse

Unigene: 204067 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.www.chomd.com.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: 最新国产成人精品不卡视频 | 色多多导航在线APP| 成人私人影院在线观看网址| 就要操就要操就要操就要操就要| 91在线视频一区201717| 国产大片在线播放高清av| 九九这里只有精品视频视网站 | 99999久久久久久亚洲一本道 | 国产白嫩漂亮美女在线观看网站| 精品一区二区三区在线成人3d动漫 | 大 香 蕉 伊 人 在 线视频| 亚洲美女大胸诱惑视频在线观看 | 搡老熟女国产1000部| 国产精品外流一区二区| 亚洲黄色中文字幕视屏拍的| 亚洲第一二三四区APP下载 | 99精品久久精品一区二区黑牛影视| 大黑人交?╳╳?视频3d| 亚洲AV无码乱码国产精品蜜芽 | 一级一级特黄女人精品毛片日胖女人 | 伊人久久综合成人网777| 久久亚洲日韩看片无码精品| 3Dh亚洲精品一区二区| 一区二区三区四区在线视频| 久久人人爽人人爽人人片av高清新婚之夜内射 | 一级毛片全部免费播放玉蒲团视频| 东北体育老师Gay粗而爽| ChⅰneSe熟女密妇乱2| 无码国产伦一区二区三区视频al换脸 | 久久99精品久久久久久久不卡,欧美伊人色综合久久天天 | 岛国无码在线播放蜜臀hd| 亚洲第一第二官网| 国产精彩免费视频资源咪咪| 羞羞视频在线观看入口污导航一区视频 | 国内大量偷窥精品视频资源| 波多野结衣中文字幕久久丝袜 | 人人妻人人澡人人爽国产一区 | 无码精品久久人妻精油按摩 | 亚洲第一网站男人都懂2023| 边吃奶边舔下面的感觉| 久久久久人妻精品一区二区色戒 |