MRPL19 cDNA ORF Clone in Cloning Vector, Human

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MRPL19 cDNA ORF Clone in Cloning Vector, Human: 产品信息

基因
种属
Human
NCBI 参考序列号
基因长度
879 bp
序列特征
Identical with the Gene Bank Ref. ID sequence.
产品特征
Full length Clone DNA of Human mitochondrial ribosomal protein L19
质粒
载体
测序引物
M13-47 and RV-M
质控
The plasmid is confirmed by full-length sequencing.
筛选
细菌筛选抗性
Ampicillin
储存 & 运输
运输方式
Each tube contains lyophilized plasmid.
储存条件
The lyophilized plasmid can be stored at ambient temperature for three months.

MRPL19 cDNA ORF 核苷酸序列及氨基酸序列信息

**Sino Biological guarantees 100% sequence accuracy of all synthetic DNA constructs we deliver, but we do not guarantee protein expression in your experimental system. Protein expression is influenced by many factors that may vary between experiments or laboratories.**

关于 MRPL19的更多信息

Entrez Gene ID

MRPL19 cDNA ORF Clone in Cloning Vector, Human: 别称

L19mt cDNA ORF Clone, Human; MRP-L15 cDNA ORF Clone, Human; MRP-L19 cDNA ORF Clone, Human; MRPL15 cDNA ORF Clone, Human; RLX1 cDNA ORF Clone, Human; RPML15 cDNA ORF Clone, Human

MRPL19 背景信息

MRPL19 (Mitochondrial Ribosomal Protein L19) is a Protein Coding gene. The MRPL19 gene, located on 2p12, is conserved in chimpanzee, Rhesus monkey, dog, cow, mouse, rat, chicken, zebrafish, fruit fly, mosquito, C.elegans, and frog. MRPL19 belongs to the bacterial ribosomal protein bL19 family. This gene encodes a 39S subunit protein and is widely expressed in the thyroid, kidney, and other tissues. Diseases associated with MRPL19 include Reading Disorder and Dyslexia. Among its related pathways are Organelle biogenesis and maintenance and Viral mRNA Translation. Data support that MRPL19 and C2ORF3 are candidate susceptibility genes for DYX3. 243 organisms have orthologs with the human gene MRPL19.
全称
mitochondrial ribosomal protein L19
参考文献
  • Paracchini S, et al. (2011) Analysis of dyslexia candidate genes in the raine cohort representing the general australian population. Genes Brain Behav 10 (2): 158-165.
  • Mascheretti S, et al. (2018) Beyond genes: A systematic review of environmental risk factors in specific reading disorder. Res Dev Disabil 82 147-152.
  • Anthoni H, et al. (2007) A locus on 2p12 containing the co-regulated mrpl19 and c2orf3 genes is associated to dyslexia. Hum Mol Genet 16 (6): 667-677.
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