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Rabbit Anti-DCUN1D4/AP Conjugated antibody (bs-14208R-AP)
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說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-14208R-AP
英文名稱 Rabbit Anti-DCUN1D4/AP Conjugated antibody
中文名稱 堿性磷酸酶(AP)標記的DCN1樣蛋白4抗體
別    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.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  免疫學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Sheep, )
產品應用 WB=1:50-200 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 34kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human DCUN1D4
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
產品介紹 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.

Similarity:
Contains 1 DCUN1 domain

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



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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