mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

掃碼關(guān)注公眾號           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
欧美日韩免费一区二区,麻豆av毛片在线观看
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-ATP6V0A2/PE-Cy3 Conjugated antibody (bs-12761R-PE-Cy3)
訂購熱線:400-901-9800
訂購郵箱:sales@m.p2b3.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@m.p2b3.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-12761R-PE-Cy3
英文名稱 Rabbit Anti-ATP6V0A2/PE-Cy3 Conjugated antibody
中文名稱 PE-Cy3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(lǐng)域 腫瘤  細胞生物  信號轉(zhuǎn)導(dǎo)  細胞分化  表觀遺傳學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Sheep, )
產(chǎn)品應(yīng)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(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 www.m.p2b3.cn 北京博奧森生物技術(shù)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
日韩午夜经典福利| 日韩美女叉B视频| 欧美人与性动交b欧美精品| 丁香社区五月在线视频久| 中文字幕人妻一区二区三区人妻| 亚洲午夜av一区二区三区| 国产日韩精品v一区二区| 最新的精品亚洲一区二区| 日本黄色美女射精| 亚洲精品伦理熟女国产| 男人把昆吧放女人屁股里| 精品区在线导航视频观看| 多男用舌头伺候一女| 美女被插进去黄色| 我想看操小嫩逼大片| 把女生操出水的视频| 久久久国产精品亚洲无码| 2021最新热播国产一区二区| 骚狐狸免费在线观看视频| 日本人色频在线看观| 欧美人与性动交b欧美精品| 午夜精品福利一区二区三区蜜桃p| 女生小穴色色视频| 国产亚洲欧美中文日韩| 亚洲卡通动漫第127页| 精品美女久久久久久嘘嘘| 欧美十八一区二区三区| 性色av少妇一区二区三区多人| 欧美高清一二三区| 搬开女人下面使劲插视频| 精品少妇一区二区三区中文字幕| 中文字幕乱码人妻一区二区三区| 日本最新免费不卡一区二区三区| 热精品韩国毛久久久久久| 女人被男人操到高潮视频| 看小伙草白女人比的黄片| 骚逼被狂插视频教程| 美国毛片亚洲社区成人看| 日韩欧美视频在线观看不卡| 添女人荫道口视频| 泡芙啪啪啪黄色污污|