MRPL3 Antibody

中文名稱：

MRPL3兔多克隆抗體
貨號(hào)：

CSB-PA003294
規(guī)格：

￥1090
圖片：
Western Blot analysis of Jurkat cells using MRP-L3 Polyclonal Antibody

Western Blot analysis of Jurkat cells using MRP-L3 Polyclonal Antibody
其他：

產(chǎn)品詳情

Uniprot No.：

P09001
基因名：

MRPL3
別名：

39S ribosomal protein L3 antibody; 39S ribosomal protein L3 mitochondrial antibody; COXPD9 antibody; L3mt antibody; Mitochondrial 39S ribosomal protein L3 antibody; Mitochondrial 60S ribosomal protein L3 antibody; mitochondrial antibody; mitochondrial ribosomal protein antibody; Mitochondrial ribosomal protein L3 antibody; MRL3 antibody; MRP-L3 antibody; MRPL3 antibody; RM03_HUMAN antibody; RPML3 antibody
宿主：

Rabbit
反應(yīng)種屬：

Human
免疫原：

Synthesized peptide derived from the Internal region of Human MRP-L3.
免疫原種屬：

Homo sapiens (Human)
標(biāo)記方式：

Non-conjugated
抗體亞型：

IgG
純化方式：

The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
產(chǎn)品提供形式：

Liquid
應(yīng)用范圍：

WB, ELISA

推薦稀釋比：

Application	Recommended Dilution
WB	1:500-1:2000
ELISA	1:5000

Protocols：

Western Blotting (WB) Protocol
ELISA Protocol
儲(chǔ)存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

基因功能參考文獻(xiàn)：
1. Found MRPL3 S75N variant is probably a rare cause of Tourette syndrome/chronic tic phenotype in Chinese Han patients. PMID: 22507240
2. the first mutation in large mitochondrial ribosomal protein MRPL3 in a family of four sibs with hypertrophic cardiomyopathy, psychomotor retardation, and multiple respiratory chain deficiency.(MRPL3) PMID: 21786366
相關(guān)疾病：

Combined oxidative phosphorylation deficiency 9 (COXPD9)
亞細(xì)胞定位：

Mitochondrion.
蛋白家族：

Universal ribosomal protein uL3 family
數(shù)據(jù)庫(kù)鏈接：

HGNC: 10379

OMIM: 607118

KEGG: hsa:11222

STRING: 9606.ENSP00000264995

UniGene: Hs.205163

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