产品中心
当前位置：首页>产品中心Anti-PRSS56/PE-Cy3
货号： bs-24096R-PE-Cy3 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-24096R-PE-Cy3
- 英文名称
- Anti-PRSS56/PE-Cy3
- 中文名称
- PE-Cy3标记的丝氨酸蛋白酶56抗体
- 别 名
- MCOP6; Protease serine 56; PRS56_MOUSE; Putative serine protease 56; Serine protease 56.
- 规格价格
- 100ul/2980元购买 大包装/询价
- 说 明 书
- 100ul
- 研究领域
- 细胞生物 发育生物学 神经生物学 干细胞
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- 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
- 63kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 2mg/1ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from mouse PRSS56
- 亚 型
- IgG
- 纯化方法
- affinity purified by Protein A
- 储 存 液
- Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.05M PB, pH 7.5.
- 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:
This gene encodes a protein that contains a peptidase S1 domain and possesses trypsin-like serine protease activity. The encoded protein may play a role in eye development, and mutations in this gene are a cause of autosomal recessive posterior microphthalmos. [provided by RefSeq, Dec 2011]
Subcellular Location:
Endoplasmic reticulum
Tissue Specificity:
Expressed neural retina, cornea, sclera and optic nerve.
DISEASE:
A developmental ocular disorder characterized by small malformed eyes. Clinical features are extreme hyperopia due to short axial length with essentially normal anterior segment, steep corneal curvatures, shallow anterior chamber, thick lenses, and thickened scleral wall. Palpebral fissures appear narrow because of relatively deep-set eyes, visual acuity is mildly to moderately reduced, and anisometropic or strabismic amblyopia is common. The fundus of the eye shows crowded optical disks, tortuous vessels, and an abnormal foveal avascular zone.
Database links:Entrez Gene: 646960 Human
Entrez Gene: 84618 Mouse
Entrez Gene: 363274 Rat
Omim: 613858 Human
SwissProt: P0CW18 Human
SwissProt: F2YMG0 Mouse
Unigene: 570310 Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.