ECHDC2 抗体 (AA 153-260)
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- 抗原 See all ECHDC2 products
- ECHDC2 (Enoyl CoA Hydratase Domain Containing 2 (ECHDC2))
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抗原表位
- AA 153-260
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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 ECHDC2 antibody is un-conjugated
- 应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)
- 预测反应
- Human,Mouse,Rat,Cow,Sheep,Pig,Horse,Zebrafish
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ECHDC2
- 亚型
- IgG
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- 应用备注
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WB 1:300-5000
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
- ECHDC2 (Enoyl CoA Hydratase Domain Containing 2 (ECHDC2))
- 别名
- ECHDC2 (ECHDC2 产品)
- 别名
- NV16396 antibody, id:ibd1032 antibody, wu:fc83b02 antibody, zgc:56321 antibody, zgc:85763 antibody, RGD1308525 antibody, 1300017C12Rik antibody, 2610009M20Rik antibody, D4Ertd765e antibody, enoyl-CoA hydratase domain containing 2 antibody, methylglutaconyl-CoA hydratase, mitochondrial antibody, enoyl CoA hydratase domain containing 2 antibody, enoyl Coenzyme A hydratase domain containing 2 antibody, ECHDC2 antibody, echdc2 antibody, LOC100121877 antibody, Echdc2 antibody
- 背景
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Synonyms: 1300017C12Rik, 2610009M20Rik, D4Ertd765e, Enoyl Coenzyme A hydratase domain containing 2, FLJ10948, Enoyl-CoA hydratase domain-containing protein 2, RGD1308525, RP23-379K6.3, ECHD2_HUMAN.
Background: ECHDC2 is a 292 amino acid mitochondrial protein that exists as two isoforms which are produced by alternative splicing events. The gene encoding ECHDC2 maps to chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome. Chromosome 1 encodes a large number of disease-associated proteins, including Lamin A which, when expressed abnormally, can build up in the nucleus and cause nuclear blebs, a characteristic of the rare aging disease Hutchinson-Gilford progeria. Additionally, genes that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinsons Disease, Gaucher disease, schizophrenia and Usher syndrome are all located on chromosome 1. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.
- 基因ID
- 55268
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