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(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務
  
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
国产农村妇女一级A片麻豆手机版,特级西西444WWW大精品视频
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-Opn1mw/Gold Conjugated antibody (bs-19646R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-19646R-Gold
英文名稱 Rabbit Anti-Opn1mw/Gold Conjugated antibody
中文名稱 膠體金標記的綠視蛋白敏感CBBM抗體
別    名 CBBM; CBD; COD5; Color blindness, deutan; Cone dystrophy 5 (X linked); GCP; GOP; Green cone photoreceptor pigment; Green cone pigment; Green sensitive opsin; Green-sensitive opsin; Medium wave sensitive; Medium wave sensitive opsin 1; Medium-wave-sensitive opsin 1; MGC176615; MGC177321; MGC198468; MGC198469; OPN1MW; OPN1MW1; OPN1MW2; OPSG_HUMAN; Opsin 1 (cone pigments), medium wave sensitive (color blindness, deutan); Opsin 1 (cone pigments), medium wave sensitive 2; Opsin 1 (cone pigments), medium wave sensitive; Photopigment apoprotein.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領(lǐng)域 神經(jīng)生物學  G蛋白偶聯(lián)受體  G蛋白信號  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應
產(chǎn)品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 40kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Opn1mw
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產(chǎn)品介紹 background:
This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called green cone photopigment or medium-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. The long-wavelength opsin gene and multiple copies of the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of deutanopic colorblindness. [provided by RefSeq, Mar 2009]

Function:
Visual pigments are the light-absorbing molecules that mediate vision. They consist of an apoprotein, opsin, covalently linked to cis-retinal.

Subcellular Location:
Membrane.

Tissue Specificity:
The three color pigments are found in the cone photoreceptor cells.

Post-translational modifications:
Phosphorylated on some or all of the serine and threonine residues present in the C-terminal region.

DISEASE:
Defects in OPN1MW are the cause of partial colorblindness deutan series (CBD) [MIM:303800]; also known as deuteranopia.
Defects in OPN1MW are a cause of blue cone monochromacy (BCM) [MIM:303700]. A rare X-linked congenital stationary cone dysfunction syndrome characterized by the absence of functional long wavelength-sensitive and medium wavelength-sensitive cones in the retina. Color discrimination is severely impaired from birth, and vision is derived from the remaining preserved blue (S) cones and rod photoreceptors. BCM typically presents with reduced visual acuity, pendular nystagmus, and photophobia. Patients often have myopia.
Defects in OPN1MW are a cause of cone dystrophy type 5 (COD5) [MIM:303700]. A X-linked cone dystrophy. Cone dystrophies are retinal dystrophies characterized by progressive degeneration of the cone photoreceptors with preservation of rod function, as indicated by electroretinogram. However, some rod involvement may be present in some cone dystrophies, particularly at late stage. Affected individuals suffer from photophobia, loss of visual acuity, color vision and central visual field. Another sign is the absence of macular lesions for many years. Cone dystrophies are distinguished from the cone-rod dystrophies in which some loss of peripheral vision also occurs.

Similarity:
Belongs to the G-protein coupled receptor 1 family. Opsin subfamily.

Database links:

Entrez Gene: 2652 Human

Entrez Gene: 728458 Human

Entrez Gene: 14539 Mouse

Entrez Gene: 89810 Rat

Omim: 300821 Human

Omim: 303800 Human

SwissProt: P04001 Human

SwissProt: O35599 Mouse

SwissProt: O35476 Rat

Unigene: 247787 Human

Unigene: 571751 Human

Unigene: 284825 Mouse

Unigene: 81056 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.rvdoil.com 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
男人狂躁女人无遮挡久久久 | 精品无人无码乱码毛片国产 | 真实乱子一区二区福利 | 极品97尤物被啪到呻吟喷水 | 成人无码特级视频在线观看 | 亚洲一区二区视频在线观看 | 波多野结衣乳视频在线观看 | 少女哔哩哔哩高清在线播放视频 | 国产高清一区二区三区 | 欧美成人在线观看诱惑 | 无码免费看在线公开视频 | 56AV国产精品久久久久久久 | 熟女系列—91Porn | 国产暴力强伦轩人妻 | 亚洲乱伦一区二区 | 国产成人毛片视频 | 国内蜜桃臀在线观看免费视频一区二区h | 免费无码婬片AAAA片 | 四川少妇搡bbbb搡bbbb | 先锋资源站最新午夜导航 | 人妻少妇嫩草被猛烈进入无码蜜桃 | 国产一级特黄AAA大片 | 四川少妇XXXX做受内谢 | h视频在线观看网站 | 国产乱码日产乱码精品精 | 黄色免费一级少妇喷水a片 色婷婷五月色综合AⅤ色欲 | 日韩精品人妻一区二区 | 免费黄色片在线播放 | 精品人妻无码一区二区三区蜜桃一 | 大地资源国精产品视频 | 国产愉拍91九色国产愉拍 | 调教丝袜在线观看91 | 稀缺小u女呦品呦视频 | 国产一起毛国产一级毛片。 | 国产无码在线观看网站27 | 真人操逼视频丰满性感内谢高清 | 国产成人AV一区二区三区在线观看 | 欧美黑人 猛猛猛 插我一区二区在线观看 | 国产午夜成人免费看片 | 特级丰满少妇一级AAAA爱毛片 | 闺产AV一区二区无码 |