ARG42814

anti-NDUFB9 antibody

anti-NDUFB9 antibody for Flow cytometry,ICC/IF,IHC-Formalin-fixed paraffin-embedded sections,Immunoprecipitation,Western blot and Human,Mouse,Rat

概述

产品描述 Rabbit Polyclonal antibody recognizes NDUFB9
反应物种 Hu, Ms, Rat
应用 FACS, ICC/IF, IHC-P, IP, WB
宿主 Rabbit
克隆 Polyclonal
同位型 IgG
靶点名称 NDUFB9
抗原物种 Human
抗原 Recombinant protein of Human NDUFB9.
偶联标记 Un-conjugated
別名 NADH-ubiquinone oxidoreductase B22 subunit; CI-B22; LYR motif-containing protein 3; B22; NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9; LYRM3; UQOR22; Complex I-B22

应用说明

应用建议
应用 推荐稀释比
FACS1:50
ICC/IF1:50
IHC-P1:50
IP1:20
WB1:1000
应用说明 * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
阳性对照 Rat brain
实际分子量 ~ 23 kDa

属性

形式 Liquid
纯化 Affinity purified.
缓冲液 50 mM Tris-Glycine (pH 7.4), 150 mM NaCl, 0.01% Sodium azide, 40% Glycerol and 0.05% BSA.
抗菌剂 0.01% Sodium azide
稳定剂 40% Glycerol and 0.05% BSA
浓度 Batch dependent
存放说明 For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项 For laboratory research only, not for drug, diagnostic or other use.

生物信息

数据库连接

GeneID: 4715 Human NDUFB9

GeneID: 66218 Mouse NDUFB9

Swiss-port # Q9CQJ8 Mouse NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9

Swiss-port # Q9Y6M9 Human NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9

基因名称 NDUFB9
全名 NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa
背景介绍 The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]
生物功能 Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed to be not involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. [UniProt]
细胞定位 Mitochondrion inner membrane; Peripheral membrane protein; Matrix side. [UniProt]
预测分子量 22 kDa

检测图片 (1) Click the Picture to Zoom In

  • ARG42814 anti-NDUFB9 antibody WB image

    Western blot: Rat brain lysate stained with ARG42814 anti-NDUFB9 antibody at 1:1000 dilution.