产品货号：
Z20978
中文名称：
MOSPD2抗体
英文名称：
Anti-MOSPD2 Antibody
产品规格：
50μl|100μl|150μl
发货周期：
1～3天
产品价格：
询价
| 抗体名称 | Anti-MOSPD2 Antibody |
| 指标别名 | MOSPD2 |
| 克隆性 | Polyclonal |
| 检验物种 | human |
| 应用范围 | WB,IHC,FCM(Intracellular),ELISA |
| 基因名称 | MOSPD2 |
| 抗体来源 | Rabbit |
| 抗体类型 | IgG |
| 免疫原 | E.coli-derived human MOSPD2 recombinant protein (Position:R111-Q496). |
| 成分 | 500μg/mL antibody with PBS，0.02% NaN3,1mg BSA and 50% glycerol. |
| 纯化方式 | Immunogen affinity purified. |
| 浓度 | 500μg/mL |
| 产品形态 | 溶液 |
| 保存条件 | 12 months from date of receipt，-20℃ as supplied.6 months 2 to 8℃ after reconstitution.Avoid repeated freezing and thawing. |
| 背景资料 | MOSPD2 (motile sperm domain-containing protein 2) is a 518 amino acid single-pass membrane protein that contains one CRAL-TRIO domain and a single MSP domain.Existing as two alternatively spliced isoforms,MOSPD2 is encoded by a gene that maps to human chromosome Xp22.2.The X and Y chromosomes are the human sex chromosomes.Chromosome X consists of about 153 million base pairs and nearly 1,000 genes.The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development.There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited,including Turner’s syndrome,Klinefelter’s syndrome and triple X syndrome.Color blindness,hemophilia,and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. |
| Uniprot ID | Q8NHP6 |
| 推荐配套试剂 | Biorab recommends Enhanced Chemiluminescent Kit with anti-Rabbit IgG (ZN1926) for Western blot,and HRP Conjugated anti-Rabbit IgG Super Vision Assay Kit (ZN1865) for IHC(P). |
| 基因名全称 | motile sperm domain containing 2 |
| 蛋白名全称 | Motile sperm domain-containing protein 2 |
| 推荐稀释比 | Western blot (WB) 1:500～2000 Immunohistochemistry (IHC) 1:50～400 Flow Cytometry(Intracellular) 1～3μg/1×106 cells Enzyme linked immunosorbent assay (ELISA) 1:100～1000 (Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
| Gene ID | 84816 |
相关搜索：MOSPD2抗体，MOSPD2多抗，Anti-MOSPD2 Antibody