NDUFS7 Polyclonal Antibody
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: NDUFS7
Target Synonym: CI 20;CI-20kD;Complex I 20kDa subunit;Complex I mitochondrial respiratory chain 20 KD subunit;Complex I-20kD;FLJ45860;FLJ46880;MGC120002;MY017;NADH coenzyme Q reductase;NADH dehydrogenase (ubiquinone) Fe S protein 7 20kDa (NADH coenzyme Q reductase);NADH dehydrogenase (ubiquinone) FeS protein 7;20kDa (NADHcoenzyme Q reductase);NADH dehydrogenase (ubiquinone) FeS protein7;20kDa (NADHcoenzyme Q reductase);NADH dehydrogenase [ubiquinone] iron-sulfur protein 7;mitochondrial;NADH-ubiquinone oxidoreductase 20 kDa subunit;NADH:ubiquinone oxidoreductase PSST subunit;NADHcoenzyme Q reductase;Ndufs7;NDUS7;PSST;PSST subunit
Research Areas: Cancer;Metabolism;Neuroscience;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse
Application: IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: O75251
Accession:
Background: This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions.
Concentration: 0.7 mg/mL
Immunogen: Recombinant protein of human NDUFS7
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: IHC 1:50-1:200
Calculated MW:
ObservedMW:
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NDUFS7 Polyclonal Antibody
NDUFS7 Polyclonal Antibody
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: NDUFS7
Target Synonym: CI 20;CI-20kD;Complex I 20kDa subunit;Complex I mitochondrial respiratory chain 20 KD subunit;Complex I-20kD;FLJ45860;FLJ46880;MGC120002;MY017;NADH coenzyme Q reductase;NADH dehydrogenase (ubiquinone) Fe S protein 7 20kDa (NADH coenzyme Q reductase);NADH dehydrogenase (ubiquinone) FeS protein 7;20kDa (NADHcoenzyme Q reductase);NADH dehydrogenase (ubiquinone) FeS protein7;20kDa (NADHcoenzyme Q reductase);NADH dehydrogenase [ubiquinone] iron-sulfur protein 7;mitochondrial;NADH-ubiquinone oxidoreductase 20 kDa subunit;NADH:ubiquinone oxidoreductase PSST subunit;NADHcoenzyme Q reductase;Ndufs7;NDUS7;PSST;PSST subunit
Research Areas: Cancer;Metabolism;Neuroscience;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse
Application: IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: O75251
Accession:
Background: This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions.
Concentration: 0.7 mg/mL
Immunogen: Recombinant protein of human NDUFS7
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: IHC 1:50-1:200
Calculated MW:
ObservedMW:
Original: $7,004,814.54
-70%$7,004,814.54
$2,101,444.36Product Information
Product Information
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Description
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: NDUFS7
Target Synonym: CI 20;CI-20kD;Complex I 20kDa subunit;Complex I mitochondrial respiratory chain 20 KD subunit;Complex I-20kD;FLJ45860;FLJ46880;MGC120002;MY017;NADH coenzyme Q reductase;NADH dehydrogenase (ubiquinone) Fe S protein 7 20kDa (NADH coenzyme Q reductase);NADH dehydrogenase (ubiquinone) FeS protein 7;20kDa (NADHcoenzyme Q reductase);NADH dehydrogenase (ubiquinone) FeS protein7;20kDa (NADHcoenzyme Q reductase);NADH dehydrogenase [ubiquinone] iron-sulfur protein 7;mitochondrial;NADH-ubiquinone oxidoreductase 20 kDa subunit;NADH:ubiquinone oxidoreductase PSST subunit;NADHcoenzyme Q reductase;Ndufs7;NDUS7;PSST;PSST subunit
Research Areas: Cancer;Metabolism;Neuroscience;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse
Application: IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: O75251
Accession:
Background: This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions.
Concentration: 0.7 mg/mL
Immunogen: Recombinant protein of human NDUFS7
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: IHC 1:50-1:200
Calculated MW:
ObservedMW:











