anti-Opsin 1 (Cone Pigments), Short-Wave-Sensitive (OPN1SW) 抗体

OPN1SW belongs to the G-protein coupled receptor 1 family, opsin subfamily. 再加上,我们可以发OPN1SW 蛋白 (3)OPN1SW 试剂盒 (1)和数多这个蛋白质的别的产品。

列出全部抗体 基因 基因ID UniProt
OPN1SW 611 P03999
OPN1SW 81644 Q63652
OPN1SW 12057 P51491
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产品编号 适用 宿主 标记 应用范围 图像 规格 供应商 交付 价格 详细
非结合性 WB <b>WB Suggested Anti-OPN1SW Antibody Titration: </b>0.2-1 ug/ml<br><b>ELISA Titer: </b>1:312500<br><b>Positive Control: </b>A549 cell lysate WB Suggested Anti-OPN1SW <br /> Antibody Titration: 0.2-1 µg/mL ELISA Titer: 1:.12500 <br /> Positive Control: A549 cell lysate <br /> OPN1SW is supported by BioGPS gene expression data to be expressed in A549 100 μL Log in to see 2至3个工作日
非结合性 WB OPN1SW antibody used at 0.2-1 ug/ml to detect target protein. 50 μg Log in to see 6至8个工作日

通过反应活性、应用领域、克隆类型和共轭标记 OPN1SW 抗体

特性 应用范围 宿主 克隆类型

Rat (Rattus)

Mouse (Murine)


Zebrafish Opsin 1 (Cone Pigments), Short-Wave-Sensitive (OPN1SW) interaction partners

  1. found a 0.3-kb region between 0.6 and 0.3 kb 5' of the SWS2 initiation codon, encompassing four cone-rod homeobox (显示 CRX 抗体)-binding sites (OTX sequences)

Guinea Pig Opsin 1 (Cone Pigments), Short-Wave-Sensitive (OPN1SW) interaction partners

  1. Changes of opsin (显示 RHO 抗体) expression might play a role in the occurrence of experimental myopia in guinea pig.

Human Opsin 1 (Cone Pigments), Short-Wave-Sensitive (OPN1SW) interaction partners

  1. LVAVA haplotype of the OPN1LW gene and MVAVA haplotype of the OPN1MW (显示 OPN1MW 抗体) gene cause apparently nonsyndromic high myopia in young patients but lead to progressive cone-rod dystrophy with deuteranopia and protanopia in middle-aged patients corresponding to a previously unknown disease course.

  2. Data suggest that insights into dimerization interface of red cone opsin should aid investigations of the structure and function of GPCR cell signaling.

  3. A novel homozygous PDE6C (显示 PDE6C 抗体) mutation was identified as the cause of ACHM. In addition, we identified an OPN1SW mutation in the sibling with complete achromatopsia.

  4. Individuals with the T190I S-opsin mutation behaved as mild tritans at 12.3-92.3Td, but as tritanopes at 1.2-9.2Td, for both light-adapted and dark-adapted conditions. The results are consistent with the mutant opsin (显示 RHO 抗体) causing abnormal S-cone function.

  5. A novel mutation(prolin/leucine) in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect.

  6. 11-cis (显示 CISH 抗体)-retinol had no significant effect on the activity of human blue cone opsin

  7. Immunoreactivity to anti-OPN1SW antibodies was seen in the upper layer of human epidermis & reconstructed skin. The opsin (显示 RHO 抗体) mRNA was seen in total RNA from human skin. Neither immunoreactivity nor mRNA expression was seen in cultured human keratinocytes.

Mouse (Murine) Opsin 1 (Cone Pigments), Short-Wave-Sensitive (OPN1SW) interaction partners

  1. These findings indicate that the aggregation of S-opsin induced by exposure to blue -emitting diode light causes endoplasmic reticulum stress, and ATF4 (显示 ATF4 抗体) activation in particular.

  2. quantitative FRET analysis in acutely isolated cone OS revealed that the cone degeneration-causing V268I mutation in peripherin-2 (显示 PRPH2 抗体) selectively reduced binding to M-opsin without affecting the peripherin-2 (显示 PRPH2 抗体) interaction to S-opsin or rhodopsin (显示 RHO 抗体)

  3. Deletion of one allele of S-opsin from Lrat (显示 LRAT 抗体)(-) (/-) mice (model of Leber congenital amaurosis) is sufficient to prevent rapid cone degeneration for at least 1 month. Deletion of both alleles of S-opsin prevents cone degeneration for at least 12 months.

  4. Thus, the three types of mouse opsin (显示 RHO 抗体) appear distinctive in the degree to which their bleached, unregenerated opsins generate "dark light."

  5. Opn1sw is a target gene for RORbeta (显示 RORB 抗体).

  6. TR beta (显示 TXNRD2 抗体) 2 and S opsin are expressed in cone photoreceptors only. Both are transcribed by E13, and their levels increase with cone genesis.

OPN1SW 抗原简介


This gene belongs to the G-protein coupled receptor 1 family, opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic.

Gene names and symbols associated with OPN1SW

  • opsin 1 (cone pigments), short-wave-sensitive 2 (opn1sw2) 抗体
  • opsin 1, short wave sensitive (OPN1SW) 抗体
  • blue-sensitive opsin (Blop) 抗体
  • KFH-B protein (kfh-b) 抗体
  • opsin 1 (cone pigments), short-wave-sensitive (opn1sw) 抗体
  • opsin 1, short wave sensitive (Opn1sw) 抗体
  • blue sensitive cone opsin (OPN2SW) 抗体
  • opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan) (Opn1sw) 抗体
  • AW551857 抗体
  • Bcp 抗体
  • Blop 抗体
  • bluops 抗体
  • BOP 抗体
  • CBT 抗体
  • CHK-2 抗体
  • GB13493 抗体
  • SI:zK13A21.5 (blue-sensitive opsin) 抗体
  • SWS1 抗体
  • SWS2 抗体
  • zfblue 抗体

Protein level used designations for OPN1SW

opsin-1, short-wave-sensitive 2 , opsin SWS-2 , blue-sensitive opsin , blue cone photoreceptor pigment , blue-sensitive visual pigment opsin , opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan) , SWS1 opsin , short-wave sensitive type 1 opsin , violet cone opsin , short-wave-sensitive (color blindness, tritan) , violet-sensitive visual pigment , opsin CHK-2 , short-wave-sensitive opsin 1 , BOP , blue cone opsin-like pigment , s opsin , short wavelength-sensitive cone opsin , cone pigment , blue opsin , Blue cone photoreceptor pigment , Blue-sensitive opsin , Short-wave-sensitive opsin 1 , S opsin , SWS opsin , UV cone pigment , blue cone opsin , blue cone pigment , blue/UV opsin , short wavelength sensitive opsin

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