DCUN1D4 抗体 (AA 161-270)
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- 抗原 See all DCUN1D4 抗体
- DCUN1D4 (DCN1, Defective in Cullin Neddylation 1, Domain Containing 4 (DCUN1D4))
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抗原表位
- AA 161-270
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适用
- 小鼠
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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 DCUN1D4 antibody is un-conjugated
- 应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human DCUN1D4
- 亚型
- IgG
- Top Product
- Discover our top product DCUN1D4 Primary Antibody
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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 - 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
- DCUN1D4 (DCN1, Defective in Cullin Neddylation 1, Domain Containing 4 (DCUN1D4))
- 别名
- DCUN1D4 (DCUN1D4 产品)
- 别名
- RGD1310422 antibody, si:ch211-14g4.1 antibody, AI836376 antibody, DCN1-like protein 4 antibody, defective in cullin neddylation 1 domain containing 4 antibody, DCN1, defective in cullin neddylation 1, domain containing 4 (S. cerevisiae) antibody, LOC100282616 antibody, LOC100283419 antibody, dcnl4 antibody, DCUN1D4 antibody, Dcun1d4 antibody, dcun1d4 antibody
- 背景
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Synonyms: DCN1, defective in cullin neddylation 1, domain containing 4, DCN1 like protein 4, DCUN1 domain containing protein 4, DCUN1D 4, KIAA0276, DCNL4_HUMAN.
Background: The DCN1-like protein family is comprised of Dcun1D1, Dcun1D2, Dcun1D3, Dcun1D4 and Dcun1D5. The founding member, Dcun1D1, is involved in the malignant transformation of squamous cell lineage.Dcun1D4, (defective in cullin neddylation protein 1-like protein 4 or DCN1-like protein 4), also designated KIAA0276, exists as 2 isoforms as a result of alternative splicing and contains one DCUN1 domain. The gene encoding Dcun1D4 maps to chromosome 4, which houses nearly 6 % of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
- 基因ID
- 23142
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