RMND1 抗体 (AA 301-400)
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- 抗原 See all RMND1 抗体
- RMND1 (Required For Meiotic Nuclear Division 1 Homolog (RMND1))
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抗原表位
- AA 301-400
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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 RMND1 antibody is un-conjugated
- 应用范围
- ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human RMND1
- 亚型
- IgG
- Top Product
- Discover our top product RMND1 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 - 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
- RMND1 (Required For Meiotic Nuclear Division 1 Homolog (RMND1))
- 别名
- RMND1 (RMND1 产品)
- 别名
- zgc:113022 antibody, DKFZp469I1433 antibody, C6orf96 antibody, COXPD11 antibody, RMD1 antibody, bA351K16 antibody, bA351K16.3 antibody, 0610042C05Rik antibody, AA408137 antibody, AI462664 antibody, AW536662 antibody, Iag-1 antibody, RGD1309546 antibody, required for meiotic nuclear division 1 homolog antibody, RMND1 antibody, rmnd1 antibody, Rmnd1 antibody
- 背景
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Synonyms: C6orf96, chromosome 6 open reading frame 96, required for meiotic nuclear division 1 homolog S. cerevisiae, Required for meiotic nuclear division protein 1 homolog, Rmnd1, RMND1_HUMAN.
Background: RMND1 is a 449 amino acid protein that belongs to the RMD1/sif2 family. Existing as three alternatively spliced isoforms, the gene encoding RMND1 maps to human chromosome 6q25.1 and mouse chromosome 10 A1. Human chromosome 6 contains 170 million base pairs and comprises nearly 6 % of the human genome. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. Additionally, Porphyria cutanea tarda, Parkinson's disease, Stickler syndrome and a susceptibility to bipolar disorder are all associated with genes that map to chromosome 6.
- 基因ID
- 55005
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