SLC7A9 抗体 (C-Term)
-
- 抗原 See all SLC7A9 抗体
- SLC7A9 (Solute Carrier Family 7 (Cationic Amino Acid Transporter, Y+ System), Member 9 (SLC7A9))
- 抗原表位
- C-Term
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This SLC7A9 antibody is un-conjugated
-
应用范围
- Western Blotting (WB)
- 交叉反应
- 人
- 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Recombinant protein encompassing a sequence within the C-terminus region of human SLC7A9. The exact sequence is proprietary.
- 亚型
- IgG
- Top Product
- Discover our top product SLC7A9 Primary Antibody
-
-
- 应用备注
- WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- 说明
-
Positive Control: human kidney
- 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1.3 mg/mL
- 缓冲液
- 1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
-
- 抗原
- SLC7A9 (Solute Carrier Family 7 (Cationic Amino Acid Transporter, Y+ System), Member 9 (SLC7A9))
- 别名
- solute carrier family 7 member 9 (SLC7A9 产品)
- 别名
- BAT1 antibody, CSNU3 antibody, 4F2-LC6 antibody, solute carrier family 7 member 9 antibody, solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 antibody, solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 L homeolog antibody, solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 antibody, SLC7A9 antibody, slc7a9 antibody, slc7a9.L antibody, Slc7a9 antibody
- 背景
- Solute carrier family 7 member 9 , BAT1 , CSNU3,This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Two transcript variants, which encode the same protein, have been found for this gene. [provided by RefSeq]
- 分子量
- 53 kDa
- 基因ID
- 11136
- UniProt
- P82251
-