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(zhì)量反饋  關于我們  聯(lián)系我們
成人h精品动漫一区二区三区,专干老熟女300部
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-CNGB3/BF594 Conjugated antibody (bs-20560R-BF594)
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-20560R-BF594
英文名稱 Rabbit Anti-CNGB3/BF594 Conjugated antibody
中文名稱 BF594標記的環(huán)核苷酸門控陽離子通道蛋白β3/CNG-β3抗體
別    名 ACHM1; ACHM3; Achromatopsia (rod monochromacy) 3; CNG channel beta-3; CNGB3; CNGB-3_HUMAN; Cone photoreceptor cGMP-gated cation channel beta-subunit; Cone photoreceptor cGMP-gated channel subunit beta; Cyclic nucleotide gated channel beta 3; Cyclic nucleotide-gated cation channel beta-3; Cyclic nucleotide-gated cation channel modulatory subunit; Cyclic nucleotide-gated channel beta-3; RMCH; RMCH1.  
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  神經(jīng)生物學  通道蛋白  細胞膜受體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Sheep, )
產(chǎn)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 92kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CNGB3
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:
Cyclic nucleotide-gated (CNG) cation channels are heteromeric complexes made up of principal alpha and modulatory beta subunits. The alpha subunits consist of CNG1-3 and form functional cation channels by themselves. The beta subunits consist of CNG4-6 and, unlike the alpha subunits, do not form functional channels, but rather modify the properties of channels. formed by CNG1-3. CNG channels are essential components of olfactory and visual transduction. CNG proteins are present in cone and rod photoreceptors and in the pineal gland, and they contribute to modulating arterial blood pressure. CNG6, also designated cyclic-nucleotide-gated cation channel beta 3 (CNG-beta 3), is an integral membrane protein that can form a heterooligomeric complex with CNG-3. CNG-beta 3 is activated by cGMP and this activation leads to the depolarization of rod photoreceptors as a result of cation channel being opened. CNG-beta 3 is expressed in a small group of retinal photoreceptor cells and in testis. Mutations in the gene encoding for CNG-beta 3, can cause achromatopsia, an autosomal recessively inherited disease characterized by low visual acuity, photophobia, a lack of color discrimination, and nystagmus.

Function:
Visual signal transduction is mediated by a G-protein coupled cascade using cGMP as second messenger. This protein can be activated by cGMP which leads to an opening of the cation channel and thereby causing a depolarization of rod photoreceptors. Induced a flickering channel gating, weakened the outward rectification in the presence of extracellular calcium, increased sensitivity for L-cis diltiazem and enhanced the cAMP efficiency of the channel when coexpressed with CNGA3 (By similarity). Essential for the generation of light-evoked electrical responses in the red-, green- and blue sensitive cones.

Subunit:
Heterooligomeric complex with CNGA3.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
Expressed specifically in the retina.

DISEASE:
Defects in CNGB3 are the cause of Stargardt disease type 1 (STGD1) [MIM:248200]. STGD is one of the most frequent causes of macular degeneration in childhood. It is characterized by macular dystrophy with juvenile-onset, rapidly progressive course, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material. STGD1 inheritance is autosomal recessive.
Defects in CNGB3 are the cause of achromatopsia type 3 (ACHM3) [MIM:262300]; also known as Pingelapese blindness. ACHM3 is a congenital complete achromatopsia and is distinct from total colorblindness mainly because of the consistent concurrence of severe myopia.

Similarity:
Belongs to the cyclic nucleotide-gated cation channel (TC 1.A.1.5) family.
CNGB3 subfamily.
Contains 1 cyclic nucleotide-binding domain.

Database links:

Entrez Gene: 54714 Human

Omim: 605080 Human

SwissProt: Q9NQW8 Human

Unigene: 154433 Human



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 m.rvdoil.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
无码区免费看一级毛片A片 中文字幕日产A片在线看 | 国产欧美精品啪啪网站 | 少妇性色生活片在线观看 | 风间由美久久久无码人妻17c | 日韩 码波多野结衣秘书 | 黑丝美女免费国产黄片 | www.maopian| 亚洲精品无码无套内射 | 午夜理理伦电影A片朋友夫妇 | 欧美性做爰又大又粗又长 | 久久久久久久久久久性爱 | 国精产品一区二区三区在线观看 | 国产精品无码不卡久久 | 美女裸体啪啪挤奶黄网站免费看 | 强奸乱伦乱码中文字幕 | 久久婷婷一级婬片A片AAA野外 | 18岁无码国内精品综合88 | 国产美女100%无裸露网站 | 国产毛多水多女人A片色情 久久AV红桃秘 一区二区 | 调教我的妺妺H肉yin荡视频 | 超碰在线免费成人WWW | 世界AV网站免费下载 | 西西4444WWW大胆无视频 | 嫩草AV无码精品一区三区 | 国产老熟女伦老熟妇A片小川桃果 | 91Porn无码国产| 欧美老熟妇BBBBB搡BBB | 欧美重囗未猛交AA片 | 奥田咲 影音先锋 亚洲一区 | www.无码爆浆蜜桃.com | 久久久久国色AV免费观看麻豆 | 国产精品久久久久久久曹县翰林府 | 亚洲精品国产成人综合久久久久久久久 | 日韩精品a在线观看 | 在线观看黄色视频国产 | www夜片内射视频日韩精品成人 | 欧美成人精品A片人妻83 | 一夲道无码专区av无码A片 | 色五月婷婷中文字幕 | 国产乱国产乱老熟300视频 | 99成人 国产精品视频 |