anti-NDUFB9 antibody

Key features and details

  • 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.
  • Brand:
CAT.NO. : ARG42814
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Product Details
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)
  • ARG42814 anti-NDUFB9 antibody WB image

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

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