验证数据展示
经过测试的应用
Positive WB detected in | Y79 cells |
推荐稀释比
应用 | 推荐稀释比 |
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Western Blot (WB) | WB : 1:200-1:1000 |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
产品信息
55183-1-AP targets PDE6C in WB, ELISA applications and shows reactivity with human samples.
经测试应用 | WB, ELISA Application Description |
经测试反应性 | human |
免疫原 | Peptide 种属同源性预测 |
宿主/亚型 | Rabbit / IgG |
抗体类别 | Polyclonal |
产品类型 | Antibody |
全称 | phosphodiesterase 6C, cGMP-specific, cone, alpha prime |
别名 | cGMP phosphodiesterase 6C, PDE6C, PDEA2 |
计算分子量 | 99 kDa |
观测分子量 | 52 kDa, 99 kDa |
GenBank蛋白编号 | NM_006204 |
基因名称 | PDE6C |
Gene ID (NCBI) | 5146 |
RRID | AB_10837359 |
偶联类型 | Unconjugated |
形式 | Liquid |
纯化方式 | Antigen affinity purification |
UNIPROT ID | P51160 |
储存缓冲液 | PBS with 0.02% sodium azide and 50% glycerol , pH 7.3 |
储存条件 | Store at -20°C. Aliquoting is unnecessary for -20oC storage. |
背景介绍
PDE6C, also named as PDEA2, belongs to the cyclic nucleotide phosphodiesterase family. It catalyze the reaction: Guanosine 3',5'-cyclic phosphate + H2O = guanosine 5'-phosphate. Defects in PDE6C are the cause of cone dystrophy type 4 (COD4). Mutations in the PDE6C gene encoding the catalytic subunit of the cone photoreceptor phosphodiesterase as a cause of autosomal recessive achromatopsia.(PMID:19887631) This antibody is specific to PDE6C.
实验方案
Product Specific Protocols | |
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WB protocol for PDE6C antibody 55183-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |