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MYPR Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN3788
产品名称
MYPR Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
PLP1 PLP
蛋白名称
MYPR
推荐应用
WB
反应种属
Human,Mouse,Rat
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
5354
Human Gene Link
https://www.uniprot.org/uniprot/5354
Human Swissprot No.
P60201
Human Swissprot Link
https://www.uniprot.org/uniprotkb/P60201/entry
Mouse Gene ID
18823
Mouse Gene Link
https://www.uniprot.org/uniprot/18823
Mouse Swissprot No.
P60202
Mouse Swissprot Link
https://www.uniprot.org/uniprotkb/P60202
Rat Gene ID
24943
Rat Gene Link
https://www.uniprot.org/uniprot/24943
Rat Swissprot No.
P60203
Rat Swissprot Link
https://www.uniprot.org/uniprotkb/P60203
免疫原
Synthesized peptide derived from human MYPR AA range: 206-256
特异性
This antibody detects endogenous levels of MYPR at Human/Mouse/Rat
稀释度
WB 1:500-2000
参考分子量
30kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene encodes a transmembrane proteolipid protein that is the predominant component of myelin. The encoded protein may play a role in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival. Mutations in this gene cause Pelizaeus-Merzbacher disease and spastic paraplegia type 2. Alternatively splicing results in multiple transcript variants, including the DM20 splice variant. [provided by RefSeq, Feb 2015],
细胞定位
Cell membrane ; Multi-pass membrane protein . Myelin membrane . Colocalizes with SIRT2 in internodal regions, at paranodal axoglial junction and Schmidt-Lanterman incisures of myelin sheat. .
功能
disease:Defects in PLP1 are the cause of leukodystrophy hypomyelinating type 1 (HLD1) [MIM:312080]; also known as Pelizaeus-Merzbacher disease. HLD1 is an X-linked recessive dysmyelinating disorder of the central nervous system in which myelin is not formed properly. It is characterized clinically by nystagmus, spastic quadriplegia, ataxia, and developmental delay.,disease:Defects in PLP1 are the cause of spastic paraplegia X-linked type 2 (SPG2) [MIM:312920]. SPG2 is characterized by spastic gait and hyperreflexia. In some patients, complicating features include nystagmus, dysarthria, sensory disturbance, mental retardation, optic atrophy.,function:This is the major myelin protein from the central nervous system. It plays an important role in the formation or maintenance of the multilamellar structure of myelin.,similarity:Belongs to the myelin proteolipid protein family.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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