FITC标记的KIAA1683蛋白抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的KIAA1683蛋白抗体

FITC标记的KIAA1683蛋白抗体

商家询价

产品名称: FITC标记的KIAA1683蛋白抗体

英文名称: Anti-KIAA1683/FITC

产品编号: HZ-17021R-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-KIAA1683/FITC Conjugated antibody

FITC标记的KIAA1683蛋白抗体

 

英文名称 Anti-KIAA1683/FITC
中文名称 FITC标记的KIAA1683蛋白抗体
别    名 K1683_HUMAN; KIAA1683; Uncharacterized protein KIAA1683.  
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  表观遗传学  
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 128kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human KIAA1683
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:
KIAA1683 is a 1,180 amino acid protein that contains six IQ domains, exists as three alternatively spliced isoforms, and is encoded by a gene that maps to human chromosome 19p13.11. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG families, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

Post-translational modifications:
Phosphorylated upon DNA damage, probably by ATM or ATR.

DISEASE:
Contains 6 IQ domains.

Similarity:
Contains 6 IQ domains.

Database links:

Entrez Gene: 80726 Human

SwissProt: Q9H0B3 Human

Unigene: 313471 Human



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

KIAA1683是一个包含六个IQ结构域的1180氨基酸蛋白,作为三个可选择的剪接异构体存在,并且由映射到人类染色体19p13.11的基因编码。由约6300万个碱基组成的1400个以上的基因,19号染色体构成了人类基因组DNA的2%以上。染色体19包括许多有趣的基因,并且被认为是人类染色体上基因密度最大的基因。它是许多免疫球蛋白超家族成员的遗传家园,包括杀伤细胞和白细胞Ig样受体、许多ICAM、CEACAM和PSG家族以及Fcα受体。眼睛颜色和头发颜色的关键基因也映射到19号染色体上。Peutz-Jeghers综合征,脊髓小脑性共济失调6型,中风病CADASIL,高胆固醇血症和胰岛素依赖型糖尿病都与染色体19有关。在一些淋巴增生性疾病中可以看到19号染色体和14号染色体的易位,典型地涉及原癌基因BCL3。