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货号： bs-19873R-AF555 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-19873R-AF555
- 英文名称
- Anti-phospho-Rhodopsin (Ser334)/AF555
- 中文名称
- AF555标记的磷酸化视网膜色素变性蛋白4抗体
- 别 名
- Rhodopsin (phospho S334); p-Rhodopsin (phospho S334); CSNBAD1; MGC138309; MGC138311; OPN 2; OPN2; opsd; OPSD_HUMAN; Opsin 2; opsin 2; Opsin 2 rod pigment; Opsin-2; Opsin2; Retinitis Pigmentosa 4; Retinitis pigmentosa 4 autosomal dominant; RHO; Rhodopsin; RP 4; RP4.
- 规格价格
- 100ul/2980元购买 大包装/询价
- 说 明 书
- 100ul
- 产品类型
- 磷酸化抗体
- 研究领域
- 细胞生物 神经生物学 信号转导 干细胞 G蛋白信号
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- Human, Rat, Rabbit,
- 产品应用
- 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
- 39kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthesised phosphopeptide derived from human Rhodopsin around the phosphorylation site of Ser334.
- 亚 型
- IgG
- 纯化方法
- affinity purified by Protein A
- 储 存 液
- 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol
- 保存条件
- 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.
- 产品介绍
- background:
Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25% of total cases, approximately 30% of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness. [provided by RefSeq, Jul 2008]
Function:
Photoreceptor required for image-forming vision at low light intensity. Required for photoreceptor cell viability after birth. Light-induced isomerization of 11-cis to all-trans retinal triggers a conformational change leading to G-protein activation and release of all-trans retinal.
Subcellular Location:
Membrane. Synthesized in the inner segment (IS) of rod photoreceptor cells before vectorial transport to the rod outer segment (OS) photosensory cilia.
Tissue Specificity:
Rod shaped photoreceptor cells which mediates vision in dim light.
Post-translational modifications:
Phosphorylated on some or all of the serine and threonine residues present in the C-terminal region.
Contains one covalently linked retinal chromophore.
DISEASE:
Retinitis pigmentosa 4.
Night blindness, congenital stationary, autosomal dominant 1
Similarity:
Belongs to the G-protein coupled receptor 1 family. Opsin subfamily.
Database links:Entrez Gene: 6010Human
Entrez Gene: 212541Mouse
Entrez Gene: 24717Rat
Omim: 180380Human
SwissProt: P08100Human
SwissProt: P15409Mouse
SwissProt: P51489Rat
Unigene: 247565Human
Unigene: 2965Mouse
Unigene: 406156Mouse
Unigene: 92530Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.