FITC标记的8号染色体开放阅读框80抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的8号染色体开放阅读框80抗体

FITC标记的8号染色体开放阅读框80抗体

商家询价

产品名称: FITC标记的8号染色体开放阅读框80抗体

英文名称: Anti-C8orf80/FITC

产品编号: HZ-20053R-FITC

产品价格: null

产品产地: 中国/上海

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: ICC=1:50-200 IF=1:50-200

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 Rabbit Anti-C8orf80/FITC Conjugated antibody 

FITC标记的8号染色体开放阅读框80抗体

 

英文名称 Anti-C8orf80/FITC
中文名称 FITC标记的8号染色体开放阅读框80抗体
别    名 C8orf80; GTPase SLIP-GC; SLIP_HUMAN; Speckled-like pattern in the germinal center.   
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 细胞生物  信号转导  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应  
产品应用 ICC=1:50-200 IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 91kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human C8orf80
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 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.
产品介绍 background:
Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf80 gene product has been provisionally designated C8orf80 pending further characterization.

Function:
Plays a role as replication-related GTPase protein in germinal center B-cell.

Subcellular Location:
Nucleus.

Tissue Specificity:
Expressed in germinal center B-cell and in lymphomas derived from germinal center B-cell.

Database links:

Entrez Gene: 389643 Human

SwissProt: Q68CJ6 Human

Unigene: 370129 Human



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

由近1亿4600万个碱基组成,8号染色体编码约800个基因。在一些白血病和淋巴瘤中发现第8染色体部分易位,并伴有c-Myc基因的扩增,并且通常与较差的预后相关。8号染色体的部分与精神分裂症和双相情感障碍有关。8三体,也称为Warkany综合征2,通常导致早期流产,但偶尔在幸存的患者中以马赛克形式出现,这些患者患有不同程度的症状,包括智力和运动发育迟缓,以及某些面部和发育缺陷。WRN是由8号染色体编码的DNA解旋酶,在早期衰老障碍沃纳综合征中显示出缺陷。第8号染色体也与菲佛综合征、先天性甲状腺功能减退症和Waord-Burg综合征有关。c8Orf80基因产物已暂时指定为C8ORF 80,有待进一步鉴定。