FITC标记的X染色体开放阅读框66抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的X染色体开放阅读框66抗体

FITC标记的X染色体开放阅读框66抗体

商家询价

产品名称: FITC标记的X染色体开放阅读框66抗体

英文名称: Anti-CXorf66/FITC

产品编号: HZ-14121R-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-CXorf66/FITC Conjugated antibody

FITC标记的X染色体开放阅读框66抗体

 

英文名称 Anti-CXorf66/FITC
中文名称 FITC标记的X染色体开放阅读框66抗体
别    名 Chromosome X open reading frame 66; Hypothetical protein LOC347487; RP11 35F15.2; Uncharacterized protein CXorf66.  
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  免疫学  发育生物学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, 
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 38kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CXorf66
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:
CXorf66 is a single-pass type I membrane protein that consists of 361 amino acids. The gene encoding CXorf66 maps to human chromosome X. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

Function:
The exact function of CXorf66 is not yet known.

Subcellular Location:
Membrane; Single-pass type I membrane protein

Database links:

Entrez Gene: 347487 Human

SwissProt: Q5JRM2 Human



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

CXOF66是由361个氨基酸组成的单通道I型膜蛋白。编码CXOF66的基因定位于人类染色体X。X和Y染色体是人类性染色体。X染色体由约1亿5300万个碱基对和近1000个基因组成。X和Y染色体的组合导致正常的男性发育,而X的两个拷贝导致正常的女性发育。存在许多与被遗传的性染色体的异常数目和组合有关的情况,包括特纳综合征、克林菲特综合征和三重X综合征。色盲、血友病和Duchenne型肌营养不良是众所周知的X染色体连锁的情况,这影响男性更频繁,因为男性携带单个X染色体。