PCSK1N 抗体 (AA 34-130)
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- 抗原 See all PCSK1N 抗体
- PCSK1N (Proprotein Convertase Subtilisin/kexin Type 1 Inhibitor (PCSK1N))
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抗原表位
- AA 34-130
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适用
- 人
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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 PCSK1N antibody is un-conjugated
- 应用范围
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human PROSAAS
- 亚型
- IgG
- Top Product
- Discover our top product PCSK1N Primary Antibody
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- 应用备注
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ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- PCSK1N (Proprotein Convertase Subtilisin/kexin Type 1 Inhibitor (PCSK1N))
- 别名
- PROSAAS (PCSK1N 产品)
- 别名
- PROSAAS antibody, SAAS antibody, Saas antibody, AI848336 antibody, KEP antibody, PEN antibody, PEN19 antibody, PEN20 antibody, Pan3 antibody, SAASCT antibody, bLEN antibody, lLEN antibody, proSAAS antibody, proprotein convertase subtilisin/kexin type 1 inhibitor antibody, PCSK1N antibody, Pcsk1n antibody
- 背景
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Synonyms: b-LEN, b-PEN-LEN, b-SAAS, Big LEN, granin like neuroendocrine peptide, l-LEN, l-SAAS, N-proSAAS, PCSK1_HUMAN, Pcsk1n, pro-SAAS, Proprotein convertase 1 inhibitor, Proprotein convertase subtilisin/kexin type 1 inhibitor, PROSAAS, SAAS, SAAS CT1-49, SAAS CT25-40.
Background: PCSK1N is a 260 amino acid protein that is both secreted and localized to the trans-Golgi network. Expressed in pancreas and brain, PCSK1N is thought to play a role in the control of the neuroendocrine secretory pathway and may also be involved in PCSK1 inhibition. The gene encoding PCSK1N maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination, as an X and a Y chromosome lead to normal male development, while two copies of an X chromosome lead to normal female development. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.
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