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富含亮氨酸重复蛋白6抗体

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产品名称: 富含亮氨酸重复蛋白6抗体
产品型号: LRRC6
产品展商: 单克隆抗体/多克隆抗体
产品文档: 无相关文档

简单介绍

富含亮氨酸重复蛋白6抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。富含亮氨酸重复蛋白6抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产品质量,质量稳定,实验效果明显。


富含亮氨酸重复蛋白6抗体  的详细介绍

富含亮氨酸重复蛋白6抗体

规格:1mg/1ml

英文名: LRRC6

别名: Leucine rich repeat containing 6; Leucine rich repeat containing protein 6; Leucine rich testis specific protein; Leucine-rich repeat-containing protein 6; Leucine-rich testis-specific protein; Lrrc6;

分子量: 54kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:Polyclonal

亚型:IgG

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human LRRC6

交叉反应:Human, Mouse, Rat, Dog, Pig, Cow, Horse, Sheep,

细胞定位:细胞浆

富含亮氨酸重复蛋白6抗体产品介绍:background: The leucine-rich repeat-containing protein 6 (LRRC6), also designated Leucine-rich testis-specific protein (LRTP), is a 466 amino acid protein that contains 3 LRR repeats and plays a role in spermatogenesis. The gene encoding LRRC6 maps to chromosome 8, which encodes approximately 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. Chromosome 8 is also associated with Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. Function: May play a role in dynein arm assembly,富含亮氨酸重复蛋白6抗体 hence essential for proper axoneme building for cilia motility. Subcellular Location: Cytoplasm. Cell projection > cilium. Tissue Specificity: Expressed predominantly in testis and in nasal epithelial cells. DISEASE: Defects in LRRC6 are the cause of primary ciliary dyskinesia 19 (CILD19) [MIM:614935]. A disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia; reduced fertility is often observed in male patients due to abnormalities of sperm tails. Half of the富含亮氨酸重复蛋白6抗体 patients exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome. Similarity: Belongs to the tilb protein family. Contains 1 CS domain. Contains 4 LRR (leucine-rich) repeats. Contains 1 LRRCT domain. Gene ID: 23639 Database links: Entrez Gene: 23639 Human Entrez Gene: 54562 Mouse Entrez Gene: 299920 Rat SwissProt: Q86X45 Human SwissProt: O88978 Mouse Unigene: 591865 Human Unigene: 244890 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

富含亮氨酸重复蛋白6抗体产品应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:细胞生物  发育生物学  干细胞  转录调节因子  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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