甲硫氨酸轉運RNA合成酶2抗體

產品貨號：

BN40531R
中文名稱：

甲硫氨酸轉運RNA合成酶2抗體
英文名稱：

Rabbit anti-MARS2 Polyclonal antibody
品牌：

Biorigin

貨號

產品規格

售價

備注
BN40531R-100ul

100ul

￥2360.00

交叉反應：Rat(predicted:Human,Mouse,Dog,Cow,Horse) 推薦應用：WB,IHC-P,IHC-F,ICC,IF,ELISA
BN40531R-200ul

200ul

￥3490.00

交叉反應：Rat(predicted:Human,Mouse,Dog,Cow,Horse) 推薦應用：WB,IHC-P,IHC-F,ICC,IF,ELISA

產品描述

英文名稱	MARS2
中文名稱	甲硫氨酸轉運RNA合成酶2抗體
別名	mars2; Methionine tRNA ligase 2; Methionine tRNA ligase 2 mitochondrial; Methionine tRNA ligase; Methionine tRNA synthetase 2; Methionine--tRNA ligase; Methionyl tRNA synthetase 2 mitochondrial; Methionyl tRNA synthetase mitochondrial; Methionyl-tRNA synthetase 2; MetRS; mitochondrial; Mitochondrial methionine tRNA ligase; Mitochondrial methionyl tRNA synthetase; Mitochondrial methionyl-tRNA synthetase; MtMetRS; SYMM_HUMAN.
研究領域	細胞生物神經生物學信號轉導轉運蛋白表觀遺傳學
抗體來源	Rabbit
克隆類型	Polyclonal
交叉反應	Rat, (predicted: Human, Mouse, Dog, Cow, Horse, )
產品應用	WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 （石蠟切片需做抗原修復） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
分子量	63kDa
細胞定位	細胞漿
性狀	Liquid
濃度	1mg/ml
免疫原	KLH conjugated synthetic peptide derived from human MARS2:31-130/593
亞型	IgG
純化方法	affinity purified by Protein A
儲存液	0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件	Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMed	PubMed
產品介紹	This gene produces a mitochondrial methionyl-tRNA synthetase protein that is encoded by the nuclear genome and imported to the mitochondrion. This protein likely functions as a monomer and is predicted to localize to the mitochondrial matrix. Mutations in this gene are associated with the autosomal recessive neurodegenerative disease spastic ataxia-3 (SPAX3). [provided by RefSeq, Apr 2014] DISEASE: Spastic ataxia 3, autosomal recessive (SPAX3) [MIM:611390]: A neurologic disorder characterized by cerebellar ataxia, ataxic gait, spasticity, and hyperreflexia. Other variable features include dysarthria, dysmetria, mild cognitive impairment, urinary urgency and dystonic positioning. Note: The disease is caused by mutations affecting the gene represented in this entry. Similarity: Belongs to the class-I aminoacyl-tRNA synthetase family. SWISS: Q96GW9 Gene ID: 92935 Database links: Entrez Gene: 92935 Human Omim: 609728 Human SwissProt: Q96GW9 Human Unigene: 116602 Human Unigene: 744330 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications