Coagulation Factor IX 抗体
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- 抗原 See all Coagulation Factor IX (F9) 抗体
- Coagulation Factor IX (F9)
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This Coagulation Factor IX antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (IF)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human Factor IX / F9 (NP_000124.1).
- 亚型
- IgG
- Top Product
- Discover our top product F9 Primary Antibody
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- 应用备注
- WB 1:500-1:2000 IF 1:50-1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- Coagulation Factor IX (F9)
- 别名
- Factor IX / F9 (F9 产品)
- 别名
- AA407498 antibody, AI506714 antibody, AK-3 antibody, Ak3l antibody, Ak3l1 antibody, Akl3l antibody, FIX antibody, HEMB antibody, P19 antibody, PTC antibody, THPH8 antibody, AW111646 antibody, Cf-9 antibody, Cf9 antibody, f9 antibody, zgc:109775 antibody, fix antibody, ptc antibody, hemb antibody, FIXA antibody, zgc:136807 antibody, adenylate kinase 3 antibody, coagulation factor IX antibody, coagulation factor IXa antibody, coagulation factor 9 antibody, coagulation factor 9 S homeolog antibody, Coagulation factor IX antibody, coagulation factor IXb antibody, Ak3 antibody, F9 antibody, f9a antibody, f9 antibody, CpipJ_CPIJ003776 antibody, CpipJ_CPIJ009129 antibody, CpipJ_CPIJ013063 antibody, CpipJ_CPIJ013624 antibody, Tsp_01441 antibody, f9.S antibody, fa9 antibody, f9b antibody
- 背景
- This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca+2 ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing.
- 分子量
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Observed_MW: 50 kDa
Calculated_MW: 47 kDa/51 kDa
- 基因ID
- 2158
- UniProt
- P00740
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