Cn|En

现货抗体产品库

DGCR8 Rabbit Polyclonal Antibody

产品详情 相关文献 产品问答 相关产品

产品基本信息

产品货号
BD-PN3390
产品名称
DGCR8 Rabbit Polyclonal Antibody
别名
Microprocessor complex subunit DGCR8 (DiGeorge syndrome critical region 8)
类别
常规抗体
基因名称
DGCR8 C22orf12 DGCRK6 LP4941
蛋白名称
DGCR8
推荐应用
WB
反应种属
Human,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.348% New type preservative N.
Human Gene ID
54487
Human Gene Link
https://www.uniprot.org/uniprot/54487
Human Swissprot No.
Q8WYQ5
Human Swissprot Link
https://www.uniprot.org/uniprotkb/Q8WYQ5/entry
Mouse Gene ID
94223
Mouse Gene Link
https://www.uniprot.org/uniprot/94223
Mouse Swissprot No.
Q9EQM6
Mouse Swissprot Link
https://www.uniprot.org/uniprotkb/Q9EQM6
免疫原
Synthesized peptide derived from human DGCR8 AA range: 467-517
特异性
This antibody detects endogenous levels of DGCR8 at Human/Mouse
稀释度
WB 1:500-2000
预测分子量
85kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene encodes a subunit of the microprocessor complex which mediates the biogenesis of microRNAs from the primary microRNA transcript. The encoded protein is a double-stranded RNA binding protein that functions as the non-catalytic subunit of the microprocessor complex. This protein is required for binding the double-stranded RNA substrate and facilitates cleavage of the RNA by the ribonuclease III protein, Drosha. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2010],
组织表达
Ubiquitously expressed.
细胞定位
Nucleus . Nucleus, nucleolus . Colocalizes with nucleolin and DROSHA in the nucleolus. Mostly detected in the nucleolus as electron-dense granular patches around the fibrillar center (FC) and granular component (GC). Also detected in the nucleoplasm as small foci adjacent to splicing speckles near the chromatin structure. Localized with DROSHA in GW bodies (GWBs), also known as P-bodies (PubMed:17159994).
功能
disease:May play a part in the etiology of the velocardiofacial/DiGeorge syndrome (VCFS/DGS), a developmental disorder characterized by structural and functional palate anomalies, conotruncal cardiac malformations, immunodeficiency, hypocalcemia, and typical facial anomalies. Most cases result from a deletion of chromosome 22q11.2 (the DiGeorge syndrome chromosome region, or DGCR).,similarity:Contains 1 WW domain.,similarity:Contains 2 DRBM (double-stranded RNA-binding) domains.,tissue specificity:Ubiquitously expressed.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

相关文献

产品问答

相关产品

免责声明| 法律支持| 联系方式

市场:027-65023363   行政/人事:027-62439686   邮箱:marketing@brainvta.com  

销售总监:张经理  18995532642  华东区:陈经理 18013970337   华南区:王经理 13100653525   华中/西区:杨经理 18186518905   华北区:张经理 18893721749

地址:中国武汉东湖高新区光谷七路128号中科开物产业园1号楼

Copyright © 武汉枢密脑科学技术有限公司. All RIGHTS RESERVED.
鄂ICP备2021009124号 DIGITAL BY VTHINK