强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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(zhì)量反饋  關于我們  聯(lián)系我們
久久99精品国产.久久久久久 ,成人羞羞 国产免费,精品人妻一区二区三区日产乱码
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-ATP6V0A2/AP Conjugated antibody (bs-12761R-AP)
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(chǎn)品編號 bs-12761R-AP
英文名稱 Rabbit Anti-ATP6V0A2/AP Conjugated antibody
中文名稱 堿性磷酸酶(AP)標記的液泡膜質(zhì)子轉(zhuǎn)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(guī)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(zhuǎn)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(chǎn)品應用 IHC-P=1:50-200 IHC-F=1:50-200 ICC=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(chǎn)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(quán)所有 2004-2026 m.nmgps.com 北京博奧森生物技術有限公司
通過國際質(zhì)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(zhì)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(wǎng)安備110107000727號
色先锋影音A∨资源网 | 特级丰满小妇免费观看 | 国产XXXX裸体XXX免费 | .www.91看片.com | 国产一区二区三区的情色影视 | 亚洲视频高清无码在线观看 | 免费A级做爰片免费视频 | 黄色成人网站在线观看 | 精品国产污网站直接看 | 尻屄视频无套内射 | 午夜精品久久久久久久91蜜桃 | 久久成人麻豆精品一牛影视 | 又粗又大又黄视频 | 精品国产黄a∨片高清在线 日韩欧美丝袜人妻自拍偷拍 | 日韩精品人妻一区二区 | 在线观看亚洲专区 | ysl蜜桃色888网站 | 蜜桃av乱码人妻一二三区 | 搡BBB,搡BBBB,搡BBBB | 午夜天堂精品久久久久 | 精品A片成人国产一区 | 成年人免费黄色视频 | 少妇高潮久久久久久潘金莲 | 亚洲精品国产av | 白丝jk糖心视频在线 | 国产人妻一区二区色情网 | 成人做爰高潮片免费看视频 | 国产露脸国语对白在线 | 18 精品 爽爽国产在线观右手 | 黃色一级A片一毛片黄欢欢春雨 | 中文无码日本一级A片人 | 国产无码av在线 | 亚洲国产成人精品无码区6080 | 国产欧美一区二区三区精品酒店 | 一线大片久久久久久久久久久久久久久18 | 正在播放长泽梓无码中出 | 16-17女人一级毛片 | 轻点灬公大JI巴又大又 | 黄污网站在线观看免费在线 | 一级毛片免费看高清经典小说 | 白丝女仆被 免费网站 |