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
久久夜色精品国产欧美乱极品,欧美丰满美乳XXⅩ高潮www
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-CNGB3/PE-Cy7 Conjugated antibody (bs-20560R-PE-Cy7)
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-PE-Cy7
英文名稱 Rabbit Anti-CNGB3/PE-Cy7 Conjugated antibody
中文名稱 PE-Cy7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 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
性一交一免一费一视一频 | 性做久久久久久久久 | 伊人久久精品一区二区三区 | 17c成人免费视频在线观看 | 国产熟妇搡BBBB搡BBBB毛片 | 6699人人人人人人人人 | 国产一级婬片A片人妖 | 亚洲午夜AV久久乱码 | 成人毛片免费在线播放 | 欧亚精品乱码久久久久久 | 亚洲av无码一区 | 无码人妻熟妇av又粗又大 | 老司机在线午夜视频 | 东南亚一级毛片高清在线 | 久久久亚洲一区二区三区 | 无码精品人妻一区二区免费看网站 | 农村妇女亂伦91山西 | 少妇性色生活片在线观看 | 水蜜桃成人A片免费观看 | 美女被 又爽 又黄视频免费观看 | 人人妻人人玩人人爽 | 黄色视频免费在线播放 | 国产裸体美女永久免费视频 | 亚洲精品一区久久久久久 | AV老司机在线观看 | 99精品国产高清在线观看 | 在线亚洲无码高清视频 | 国产精品aⅴ久久久久久鸭绿欲 | 国产一级片在线观看网站 | 国产做爰又粗又大又大 | 三级在线观看午夜福利 | 国产大几把一二三 | 久久久久久久国产精品 | 97人妻人人揉人人躁人人爽动漫 | 在线一区二区三区四区 | 精品秘 无码一区二区三区老师 | 久久精品久久久久久久 | 波多野结衣亚洲色 | Xiao77熟女精品视频 | 精品国产大片大片大片 | 91人妻人人澡人人爽人人精品乱 |