MNX1 抗体 (AA 242-271)
Quick Overview for MNX1 抗体 (AA 242-271) (ABIN5535259)
抗原
See all MNX1 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 242-271
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纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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免疫原
- This MNX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 242-271 amino acids from the Central region of human MNX1.
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亚型
- Ig Fraction
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anti-Motor Neuron and Pancreas Homeobox 1 (MNX1) (AA 330-380) antibody
MNX1 适用: 人, 小鼠, 大鼠 WB, IHC (p), IHC 宿主: 兔 Polyclonal unconjugated
anti-Motor Neuron and Pancreas Homeobox 1 (MNX1) (AA 231-330) antibodyMNX1 适用: 人, 大鼠 WB, ELISA, FACS, IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Motor Neuron and Pancreas Homeobox 1 (MNX1) (AA 50-99) antibodyMNX1 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Motor Neuron and Pancreas Homeobox 1 (MNX1) (C-Term) antibodyMNX1 适用: 人, 小鼠, 大鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Motor Neuron and Pancreas Homeobox 1 (MNX1) (AA 251-300) antibodyMNX1 适用: 人, 小鼠, 大鼠, Pig, 豚鼠, 马, 兔, 小鸡 WB 宿主: 兔 Polyclonal unconjugated
anti-Motor Neuron and Pancreas Homeobox 1 (MNX1) (AA 36-85) antibodyMNX1 适用: 人, 小鼠, 犬 WB 宿主: 兔 Polyclonal unconjugated
anti-Motor Neuron and Pancreas Homeobox 1 (MNX1) antibodyMNX1 适用: 人 WB 宿主: 兔 Monoclonal unconjugated
anti-Motor Neuron and Pancreas Homeobox 1 (MNX1) antibodyMNX1 适用: 小鼠 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
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应用备注
- For WB starting dilution is: 1:1000
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.5 mg/mL
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缓冲液
- Supplied in PBS with 0.09 % (W/V) sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
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- MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))
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别名
- MNX1
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背景
- This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq].
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分子量
- 41 kDa
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基因ID
- 3110
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UniProt
- P50219
抗原
-
