HFE 抗体 (N-Term)
Quick Overview for HFE 抗体 (N-Term) (ABIN634556)
抗原
See all HFE 抗体适用
宿主
克隆类型
标记
应用范围
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                                            抗原表位
- N-Term
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                                            特异性
- HFE antibody was raised against the N terminal of HFE
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                                            纯化方法
- Affinity purified
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                                            免疫原
- HFE antibody was raised using the N terminal of HFE corresponding to a region with amino acids MGASEQDLGLSLFEALGYVDDQLFVFYDHESRRVEPRTPWVSSRISSQMW
 
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                                            应用备注
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                        WB: 1 µg/mL
 Optimal conditions should be determined by the investigator.
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                                            说明
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                        HFE Blocking Peptide, (ABIN5613998), is also available for use as a blocking control in assays to test for specificity of this HFE antibody 
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                                            限制
- 仅限研究用
 
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                                            状态
- Lyophilized
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                                            溶解方式
- Lyophilized powder. Add distilled water for a 1 mg/mL concentration of HFE antibody in PBS
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                                            浓度
- Lot specific
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                                            缓冲液
- PBS
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                                            注意事项
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                        Avoid repeated freeze/thaw cycles. 
 Dilute only prior to immediate use.
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                                            储存条件
- 4 °C/-20 °C
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                                            储存方法
- Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
 
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    - HFE (Hemochromatosis (HFE))
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                                            别名
- HFE
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                                            背景
- HFE is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin (beta2M). It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin. The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in its gene.
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                                            分子量
- 40 kDa (MW of target protein)
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                                            途径
- Transition Metal Ion Homeostasis, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process
 抗原
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