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Rabbit Anti-SPOCD1  antibody (bs-17682R)  
~~~促銷代碼KT202411~~~
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產(chǎn)品編號(hào) bs-17682R
英文名稱 Rabbit Anti-SPOCD1  antibody
中文名稱 SPOCD1蛋白抗體
別    名 FLJ25348; RP11-84A19.1; SPOC domain-containing protein 1; SPOC1_HUMAN; SPOCD1.  
研究領(lǐng)域 腫瘤  細(xì)胞生物  免疫學(xué)  神經(jīng)生物學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human)
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=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.
理論分子量 130kDa
細(xì)胞定位 細(xì)胞核 細(xì)胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SPOCD1: 361-450/1216 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項(xiàng) This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 SPOCD1 is a 1,216 amino acid protein that contains one SPOC domain and one TFIIS central domain. SPOCD1 exists as five alternatively spliced isoforms, with isoform 1 showing expression in lung. The gene that encodes SPOCD1 contains 25,630 bases and maps to human chromosome 1p35.2. Spanning about 260 million base pairs and making up 8% of the human genome, chromosome 1 is the largest human chromosome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1 and aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

Similarity:
Contains 1 SPOC domain.
Contains 1 TFIIS central domain.

SWISS:
Q6ZMY3

Gene ID:
90853

Database links:

Entrez Gene: 90853 Human

SwissProt: Q6ZMY3 Human

Unigene: 62604 Human



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