combination of fundus hypopigmentation, decreased visual acuity due to foveal hypoplasia, nystagmus, astigmatism, protan color vision defect, myopia, and defective dark adaptation. Except for progression of axial myopia, the disease can be co
nsidered to be a statio
nary condition. Electroretinography reveals abnormalities in both photopic and scotopic functions.
Similarity : Belo
ngs to the calcium channel alpha-1 subunit (TC 1.A.1.11) family. CACNA1F subfamily.
Databa
se l
inks : UniProtKB/Swiss-Prot: O60840.2
英文名称 Anti-C20orf196
中文名称 20号染色体开放阅读框196抗体
别 名 C20orf196; CT196_HUMAN; Uncharacterized protein C20orf196.
浓 度 1mg/1ml
规 格 0.2ml/200μg
抗体来源 Rabbit
克隆类型 polyclonal
交叉反应 Human, Mouse, Rat, Dog
产品类型 一抗
研究领域 细胞生物 免疫学 发育生物学 神经生物学
蛋白分子量 predicted molecular weight: 23kDa
性 状 Lyophilized or Liquid
酸洗玻璃珠系列10g价格免 疫 原 KLH co
njugated synthetic peptide derived from human C20orf196
亚 型 IgG
纯化方法 affinity purified by Protein A
储 存 液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
产品应用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500