Coagulation Factor IX 抗体
Quick Overview for Coagulation Factor IX 抗体 (ABIN7670576)
抗原
See all Coagulation Factor IX (F9) 抗体适用
宿主
克隆类型
标记
应用范围
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原理
- Factor IX/PTC/F9 Polyclonal Antibody(Capture/Detector)
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纯化方法
- Antigen Affinity Purification
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免疫原
- Recombinant Human Factor IX/PTC/F9 protein expressed by Mammalian
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亚型
- IgG
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anti-Coagulation Factor IX (F9) (AA 29-192) antibody
F9 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Coagulation Factor IX (F9) (AA 96-190) antibodyF9 适用: 人 WB, ELISA, IP, RNAi 宿主: 小鼠 Monoclonal 2C9 unconjugated
anti-Coagulation Factor IX (F9) (AA 144-239) antibodyF9 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Coagulation Factor IX (F9) antibodyF9 适用: 人, 小鼠, 大鼠 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Coagulation Factor IX (F9) antibodyF9 适用: 人 ELISA, IHC, IHC (p), IEP 宿主: 山羊 Polyclonal unconjugated
anti-Coagulation Factor IX (F9) (C-Term) antibodyF9 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Coagulation Factor IX (F9) antibodyF9 适用: 人 ICC, IHC (p), IF 宿主: 兔 Polyclonal unconjugated
anti-Coagulation Factor IX (F9) (AA 232-455) antibodyF9 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Coagulation Factor IX (F9) (AA 412-461) antibodyF9 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
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应用备注
- ELISA Capture 2-8 μg/mL,ELISA Detector 0.1-0.4 μg/mL
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限制
- 仅限研究用
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浓度
- 1 mg/mL
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缓冲液
- Sterile PBS , pH 7.4
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储存液
- Without preservative
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注意事项
- Avoid freeze / thaw cycles. This preparation contains no preservatives, thus it should be handled under aseptic conditions.
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储存条件
- 4 °C,-20 °C
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储存方法
- Store at 4°C Valid for 1 month or -20°C Valid for 12 months
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有效期
- 12 months
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- Coagulation Factor IX (F9)
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别名
- F9
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背景
- HEMB,P19,PTC,THPH8,Christmas Factor,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.
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UniProt
- P00740
抗原
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