| 产品名称： | Hemoglobin alpha Antibody |
| 说明书： | 【点击查看详细说明及参考图片】 |
| 货号： | 251337 |
| 规格： | 0.1 mg |
| 产品描述： | Hemoglobin alpha is involved in oxygen transport from the lung to the various peripheral tissues. Defects in hemoglobin alpha are the cause of alpha-thalassemia (A-THAL). The thalassemias are the most common monogenic diseases and occur mostly in Mediterranean and Southeast Asian populations. The hallmark of alpha-thalassemia is an imbalance in globin-chain production in the adult HbA molecule. The level of alpha chain production can range from none to very nearly normal levels. Untreated, most patients die in childhood or early adolescence. |
| 克隆类型： | Rabbit Polyclonal Antibody |
| 亚型： | Rabbit Ig |
| 免疫原： | KLH-conjugated synthetic peptide encompassing a sequence within the center region of human hemoglobin alpha. |
| 适用物种： | H, M, R, B, Ck |
| 应用范围： | E, WB, IHC |
| 应用说明： | E: 1:500-1:1,000; WB: 1:100-1:500; IHC: 1:100-1:500 |
| 别名： | HBA1; Hemoglobin alpha; Hemoglobin alpha 1; Hemoglobin subunit alpha; Hemoglobin alpha chain; Alpha-globin; HBA1 |
| 形态： | Each vial contains 0.1 mg IgG in 0.1 ml (1 mg/ml) of PBS pH7.4, 25% glycerol, 0.1 mg/ml BSA with 0.09% sodium azide. Antibody was purified by Protein-A affinity chromatography. |
| 保存条件： | Store at -20°C. Minimize freeze-thaw cycles. Product is guaranteed one year from the date of shipment. |
| 参考文献： |
