产品介绍：
产品说明
一般描述
Homogentisate 1,2-dioxygenase (HGD) gene mutations are the molecular cause of alkaptonuria, a rare hereditary disorder of the phenylalanine catabolism. The highest expression of HGD is in the prostate, small intestine, colon, and liver. The HGD gene contains 14 exons. Conflicting reports have placed the gene at 3q2, 3q13.3-q21, 3q21-q24, 3q21-q23, or 3q25-q26. (provided by RefSeq)
免疫原
HGD (NP_000178, 377 a.a. ~ 445 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Sequence
CFEKASKVKLAPERIADGTMAFMFESSLSLAVTKWGLKASRCLDENYHKCWEPLKSHFTPNSRNPAEPN
外形
Solution in phosphate buffered saline, pH 7.4
基本信息
| NACRES | NA.41 |
产品性质
| 生物来源 | mouse |
| 偶联物 | unconjugated |
| 抗体形式 | purified immunoglobulin |
| antibody product type | primary antibodies |
| 克隆 | 2C10, monoclonal |
| 形式 | buffered aqueous solution |
| 分子量 | antigen ~33.7 kDa |
| species reactivity | human |
| technique(s) | capture ELISA: suitable immunofluorescence: suitable immunoprecipitation (IP): suitable indirect ELISA: suitable |
| 同位素/亚型 | IgG2bκ |
| NCBI登记号 | NM_000187 |
| UniProt登记号 | Q93099 |
| 运输 | dry ice |
| 储存温度 | −20℃ |
| Gene Information | human ... HGD(3081) |
安全信息
| 储存分类代码 | 13 - Non Combustible Solids |
| WGK | WGK 1 |
| 闪点(F) | Not applicable |
| 闪点(C) | Not applicable |
