验证数据展示
Planning an IHC experiment? We recommend our IHCeasy HBB Ready-To-Use IHC Kit. HBB primary antibody included.
产品信息
19991-1-AP targets HBB-Specific in ELISA applications and shows reactivity with human samples.
| 经测试应用 | ELISA Application Description |
| 经测试反应性 | human |
| 免疫原 |
Peptide 种属同源性预测 |
| 宿主/亚型 | Rabbit / IgG |
| 抗体类别 | Polyclonal |
| 产品类型 | Antibody |
| 全称 | hemoglobin, beta |
| 别名 | beta globin, CD113t C, HBB, Hemoglobin beta chain, Hemoglobin subunit beta, hemoglobin, beta |
| 计算分子量 | 16 kDa |
| GenBank蛋白编号 | NM_000518 |
| 基因名称 | HBB |
| Gene ID (NCBI) | 3043 |
| 偶联类型 | Unconjugated |
| 形式 | Liquid |
| 纯化方式 | Antigen affinity purification |
| UNIPROT ID | P68871 |
| 储存缓冲液 | PBS with 0.02% sodium azide and 50% glycerol, pH 7.3. |
| 储存条件 | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
HBB, also named as LVV-hemorphin-7, CD113t-C and beta-globin, Belongs to the globin family. HBB is involved in oxygen transport from the lung to the various peripheral tissues. HBB potentiates the activity of bradykinin, causing a decrease in blood pressure. Defects in HBB may be a cause of Heinz body anemias. Defects in HBB are the cause of beta-thalassemia (B-THAL). Defects in HBB are the cause of sickle cell anemia. Defects in HBB are the cause of beta-thalassemia dominant inclusion body type (B-THALIB). The antibody has no cross reaction with HBD.
