PMP22 抗体
Quick Overview for PMP22 抗体 (ABIN6944620)
抗原
See all PMP22 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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交叉反应
- 人, 小鼠, 大鼠
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纯化方法
- Purified by Protein A.
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免疫原
- Full length protein
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亚型
- IgG
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anti-Peripheral Myelin Protein 22 (PMP22) (AA 101-160) antibody
PMP22 适用: 大鼠, 小鼠 WB, ELISA, IF (cc), IF (p), IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Peripheral Myelin Protein 22 (PMP22) (C-Term) antibodyPMP22 适用: 人, 大鼠, 小鼠 WB, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Peripheral Myelin Protein 22 (PMP22) (AA 1-64) antibodyPMP22 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Peripheral Myelin Protein 22 (PMP22) (C-Term) antibodyPMP22 适用: 人 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Peripheral Myelin Protein 22 (PMP22) (AA 31-133) antibodyPMP22 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Peripheral Myelin Protein 22 (PMP22) (AA 31-133) antibodyPMP22 适用: 人 WB, IHC, IP, ICC 宿主: 小鼠 Monoclonal C2 unconjugated
anti-Peripheral Myelin Protein 22 (PMP22) (AA 32-64) antibodyPMP22 适用: 人 ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Peripheral Myelin Protein 22 (PMP22) antibodyPMP22 适用: 大鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Peripheral Myelin Protein 22 (PMP22) (C-Term) antibodyPMP22 适用: 人, 大鼠, 小鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Peripheral Myelin Protein 22 (PMP22) (AA 27-76) antibodyPMP22 适用: 人, Cow, 豚鼠, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
FCM 1:20-100
IHC-P 1:200-400
IF(IHC-P) 1:50-200
IF(ICC) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 1xTBS ( pH 7.4), 1 % BSA, 40 %Glycerol and 0.05 % Sodium Azide.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C for 12 months.
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有效期
- 12 months
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- PMP22 (Peripheral Myelin Protein 22 (PMP22))
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别名
- PMP22
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背景
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Synonyms: Peripheral myelin protein 22, Growth arrest-specific protein 3, PMP-22, GAS-3, PMP22, GAS3
Background: PMP22 is a 22 kDa glycoprotein expressed in the compact myelin of the peripheral nervous system. In the peripheral nervous system, PMP 22 is produced by myelinating Schwann cells and is coexpressed with the genes for myelin basic protein (MBP) during nerve development and regeneration. Alterations in the level of this protein cause several genetic human diseases. If the protein is duplicated, patients develop Charcot Marie Tooth disease. If one copy of the gene is deleted, they suffer from the inherited tendency to pressure palsies.
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基因ID
- 5376
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UniProt
- Q01453
抗原
-
