LMBRD1 抗体 (C-Term)
Quick Overview for LMBRD1 抗体 (C-Term) (ABIN6991441)
抗原
See all LMBRD1 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- C-Term
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纯化方法
- LMBRD1 Antibody is affinity chromatography purified via peptide column.
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免疫原
- LMBRD1 antibody was raised against an 18 amino acid synthetic peptide near the carboxy terminus of human LMBRD1. The immunogen is located within the last 50 amino acids of LMBRD1.
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亚型
- IgG
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anti-LMBR1 Domain Containing 1 (LMBRD1) (AA 6-100) antibody
LMBRD1 适用: 人 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-LMBR1 Domain Containing 1 (LMBRD1) (AA 220-300) antibodyLMBRD1 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-LMBR1 Domain Containing 1 (LMBRD1) (C-Term) antibodyLMBRD1 适用: 人, 小鼠, 大鼠 WB, EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
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LMBRD1 antibody can be used for detection of LMBRD1 by Western blot at 1 μ,g/mL. Antibody can also be used for immunohistochemistry starting at 2.5 μ,g/mL. For immunofluorescence start at 20 μ,g/mL.
Antibody validated: Western Blot in human samples, Immunohistochemistry in human samples and Immunofluorescence in human samples. All other applications and species not yet tested. -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- LMBRD1 Antibody is supplied in PBS containing 0.02 % 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
- -20 °C,4 °C
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储存方法
- LMBRD1 antibody can be stored 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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- LMBRD1 (LMBR1 Domain Containing 1 (LMBRD1))
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别名
- LMBRD1
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背景
- LMBRD1 Antibody: LMBRD1, also known as NESI (nuclear export signal-interacting protein, is a lysosomal membrane protein that is thought be involved in the transport and metabolism of cobalamin. LMBRD1 was initially identified as interacting with the large form of the hepatitis delta antigen and may be required for the nucleocytoplasmic shuttling of the hepatitis delta virus. Mutations in this gene are associated with the vitamin B12 metabolism disorder termed, homocystinuria-megaloblastic anemia complementation type F (cblF).
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基因ID
- 55788
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NCBI登录号
- NP_060838
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UniProt
- Q9NUN5
抗原
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