KD-Validated NDUFB9 Recombinant Rabbit Monoclonal Antibody

KD-Validated NDUFB9 Recombinant Rabbit Monoclonal Antibody

Cat. No.: KVAb01014
Size:20μL Price:$118
Size:50μL Price:$218
Size:100μL Price:$318
Application:WB,FCM,ICC,IHC-P

Reactivity:Human,Mouse,Rat
Conjugate:Unconjugated
Gene Name:NDUFB9
Category: KO&KD Validated Antibodies Tags: , , , , , , , , ,

Summary

Production Name

KD-Validated NDUFB9 Recombinant Rabbit Monoclonal Antibody

Description

KD-Validated antibody

Host

Rabbit

Application

WB,FCM,ICC,IHC-P

Reactivity

Human,Mouse,Rat

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

Rabbit IgG

Clonality

Rabbit mAb

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.

Purification

Affinity purification

 

Immunogen

Gene Name

NDUFB9

Alternative Names

NADH:Ubiquinone Oxidoreductase Subunit B9; UQOR22; LYRM3; B22; NADH Dehydrogenase (Ubiquinone) 1 Beta Subcomplex, 9, 22kDa; NADH Dehydrogenase [Ubiquinone] 1 Beta Subcomplex Subunit 9; NADH-Ubiquinone Oxidoreductase B22 Subunit; LYR Motif-Containing Protein 3; Complex I B22 Subunit; CI-B22; NADH Dehydrogenase (Ubiquinone) 1 Beta Subcomplex, 9 (22kD, B22); Complex I-B22; MC1DN24

Gene ID

4715

SwissProt ID

Q9Y6M9

 

Application

Dilution Ratio

WB 1:1,000-1:5,000; FC 1:200-1:2,000; ICC 1:100-1:1,000; IHC-P 1:100-1:200

Molecular Weight

Calculated MW: 21.8kDa

 

Background

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]

 

Research Area

Metabolism

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