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NDUFA9 Recombinant Rabbit Monoclonal Antibody [PSH14-08] (HA723598)

Price: Regular price $385.00

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Catalog# HA723598

Rabbit Monoclonal to NDUFA9

Tested for

  • WB

  • IP

Reacts with

  • Human

  • Mouse

  • Rat

  • Monkey

Recombinant production enables lot-to-lot consistency and is animal-cruelty-free

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Specifications

Product Type

Recombinant Rabbit monoclonal primary

Product Name

NDUFA9 Recombinant Rabbit Monoclonal Antibody [PSH14-08] (HA723598)

Immunogen

Recombinant protein within human ndufa9 aa 1-230.

Host

Rabbit

Positive Control

HepG2 cell lysate, HeLa cell lysate, U-2 OS cell lysate, Caco-2 cell lysate, COS-1 cell lysate, NIH/3T3 cell lysate, Neuro-2a cell lysate, C6 cell lysate, L6 cell lysate, Mouse liver tissue lysate, Rat liver tissue lysate, Mouse skeletal muscle tissue lysate, Rat skeletal muscle tissue lysate.

Conjugation

Unconjugated

Clonality

Monoclonal

Clone Number

PSH14-08

APPLICATION DILUTION

  • WB

  • 1:5,000

  • IP

  • 1-2μg/sample

PROPERTIES

Form

Liquid

Storage Condition

Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.

Storage Buffer

PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.

Concentration

1ug/ul

Purification

Protein A affinity purified.

Molecular Weight

Predicted band size: 43 kDa

Isotype

IgG

TARGET

UNIPROT #

Q16795

PROTEIN NAME

NDUFA9

SYNONYMS

CI-39kD antibody;Complex I subunit NDUFA9 antibody;Complex I-39kD antibody;mitochondrial antibody;NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9 antibody;NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9 mitochondrial antibody;NADH Ubiquinone Oxidoreductase 1 alpha subcomplex 9 antibody;NADH-ubiquinone oxidoreductase 39 kDa subunit antibody;NDUA9_HUMAN antibody;NDUFA9 antibody

SUBCELLULAR LOCATION

Mitochondrion matrix.

FUNCTION

NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9 is an enzyme that in humans is encoded by the NDUFA9 gene. The NDUFA9 protein is a subunit of NADH:ubiquinone oxidoreductase (Complex I of the electron transport chain), which is located in the mitochondrial inner membrane and is the largest of the five complexes of the electron transport chain. Mutations in NADH dehydrogenase (ubiquinone), also known as Complex I, frequently lead to complex neurodegenerative diseases such as Leigh's syndrome. In the case of NDUFA9, a mutation to the MT-ND3 gene might interrupt their interaction and formation of subcomplexes, compromising Complex I function and leading to disease.

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