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 www.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
91在线无码精品秘 蜜桃按摩 | 亚洲国产无码在线视频 | 久久国产精品波多野结衣AV孕妇 | 97人妻人人揉人人澡人人下载 | 偷窥国产肥熟女一区二区 | 精精国产ⅩXXX在线观看 | 精品3d里番一二三区视频 | 69久蜜桃人妻无码精品一区 | A片男女色情A片免费姬媚直播 | 人妻体内谢精无码视频 | 色情网站在线播放免费 | 亚洲成人精品在线 | 国产成人a亚洲精品 | 久久久久国产一区二区三区 | 无码AV一区二区在线观看美腿 | 久久成人毛片又大又黄又粗又硬 | 亚洲第一影院无码久久人妻 | 亚洲精品无码AV片影音先锋在线 | 国产亲妺妺乱视频免费看 | 曰韩少妇Av又粗又大 | 蜜桃av色偷偷av老熟女 | 一级婬片试看120分钟 | 无码人妻丰满熟妇区毛片老年人 | 久久久精品人妻一区三区蜜桃 | 激情放荡性小说在线视频xx | 成人A片一区二区免费看 | 91在线无码精品秘 竹菊 | 久久久九九九精品AAA片黃色 | 国产精品昆明久久久综合888 | 中文在线一区二区 | 高清无码在线免费播放 | 欧美性猛交老妇一级A片 | 日韩视频在线免费观看 | 少妇做爰特黄A片免费看9 | 亚洲国产精品无码久久久久久久久久久 | 女人自慰冒白浆在线观看 | 91丰艺裸体歌舞无码 | 免费体验爆乳美女爱爱视频 | 人妻久久久精品996系列A片 | 69精品久久久久久久 | 国产成人A片大片免费 |