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產(chǎn)品中心抗體Polyclonal AntibodyK106562PAnti-RSL1D1 Polyclonal Antibody
產(chǎn)品型號：K106562P
更新時(shí)間：2022-08-15
廠商性質(zhì)：生產(chǎn)廠家
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產(chǎn)品分類
Anti-RSL1D1 Polyclonal Antibody
| 英文名稱 | Anti-RSL1D1 Polyclonal Antibody |
|---|---|
| 宿主 | Rabbit |
| 別名 | MEL-1A-R;MT1;MTNR1A;Melatonin receptor type 1A |
| 應(yīng)用 | WB |
| 稀釋比例 | WB 1:3000. |
| 交叉反應(yīng) | Human Mouse Rat |
| 蛋白分子量 | 60kDa |
| Gene ID | 26156 |
| 保存 | Store at -20°C. Avoid freeze / thaw cycles. |
| 儲存液 | Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3. |
| 純化方法 | Affinity purification |
| 亞型 | IgG |
| 免疫原 | A synthetic peptide of human RSL1D1 |
| 性狀 | 液體 |
| Public Immunogen Range | A synthetic peptide of human RSL1D1 |
| Subcellular Locations | Nucleus |
| Swiss Prot | P48039 |
| 克隆類型 | Polyclonal Antibody |
| 背景資料 | RSL1D1, also known as CATX-11, PBK1, L12 or CSIG, is a 490 amino acid nuclear protein that belongs to the ribosomal protein L1P family. Expressed in placenta, RSL1D1 contains many phosphorylated amino acid residues and is encoded by a gene that maps to human chromosome 16p13.13. Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. |
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