91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
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
欧美黑人一级爽快片婬片高清,搡老女人老91妇女老熟女,日本不卡在线观看
首頁 > 產品中心 > 一抗 > 產品信息
ATP6V0A2 Rabbit pAb (bs-12761R)  
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
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產品編號 bs-12761R
英文名稱 ATP6V0A2 Rabbit pAb
中文名稱 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.  
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,Pig,Sheep,Cow,Dog,Horse)
產品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 98 kDa
檢測分子量
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ATP6V0A2: 1-100/856 <Cytoplasmic>
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 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.

SWISS:
Q9Y487

Gene ID:
23545

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



版權所有 2004-2026 m.rvdoil.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
久久亚洲AV无码日韩一区二区 | 99精品国产高清在线观看 | 男女激情动图麻豆视频 | 国产精品久久久久久久午夜 | 中文字幕无码A片一区在线观看 | 西西西444WWW无码视频软件 | 欧美精品一区在线观看 | 亚洲一区二区五十路激情中出自拍 | 久久久 成人网站免费观看 人人爽人爽爽人人爽爽人人 | 91色视频免费观看 | 卡通欧美另类小说在线观看 | 激情小说激情图片激情视频QVOD | 国产乱free国语对白 | 四川一级毛毛片免费网站 | 欧美BBw搡BBBB槡BBBB | 中文在线字幕观看 | 影音先锋AV成人资源站在线播放 | 欧一美一交一配一交一交一视频 | 免费黄色成人网站在线看 | 国产精品高潮玲珑久久AV无码 | 手机大片福利社亚洲天堂 | 漂亮女大学一级毛片视频 | 国产亚洲无码视频精品 | 免费观看成人毛片A片小说 少妇的BBBB爽爽爽自慰 | 亚洲无码久久综合 | bLacK欧美黑鸡巴操逼 | 91九色视频在线观看 | 久久99精品国产自在现线 | 亚洲伊人影院一区综合 | 国产精品久久久久久久曹县翰林府 | 西西大胆一级裸体A片 | 嫩嫩BBBBBBBBB免费网站 | 久久成年人视频免费 | 影音先锋成人资源AV在线观看 | 国语对白做受 欧美 | 91在线无码精品秘 入口九 | 影音先锋av男人资源在线播放 | 日本公妇乱偷中文字幕 | 日本在线视频免费观看 | 国产免费网站无码观看 | 国产欧美一区二区三区特黄手机版 |