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Rabbit Anti-DCUN1D4  antibody (bs-14208R)
~~~促销,代码KX240301~~~
~~~促销,代码KX240302~~~
订购热线:400-901-9800
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订购QQ:  400-901-9800
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说明书: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价
产品编号 bs-14208R
英文名称 DCUN1D4
中文名称 DCN1样蛋白4抗体
别    名 DCN1 like protein 4; DCN1, defective in cullin neddylation 1, domain containing 4 (S. cerevisiae); DCN1, defective in cullin neddylation 1, domain containing 4; DCN1-like protein 4; DCNL4_HUMAN; DCUN1 domain containing protein 4; DCUN1 domain-containing protein 4; DCUN1D 4; Dcun1d4; Defective in cullin neddylation protein 1-like protein 4; KIAA0276.  
研究领域 肿瘤  细胞生物  免疫学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 (predicted: Human,Mouse,Rat,Dog,Pig,Cow,Horse,Sheep)
产品应用 IHC-P=1:100-500, IHC-F=1:100-500, ICC=1:100-500, IF=1:100-500, ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 34kDa
细胞定位 细胞核 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human DCUN1D4: 201-292/292 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 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.

Similarity:
Contains 1 DCUN1 domain

SWISS:
Q92564

Gene ID:
23142

Database links:

Entrez Gene: 23142 Human

Entrez Gene: 100737 Mouse

Entrez Gene: 360928 Rat

Omim: 612977 Human

SwissProt: Q92564 Human

SwissProt: Q8CCA0 Mouse

Unigene: 605388 Human

Unigene: 220312 Mouse



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