Search results for COX11, Cytochrome C Oxidase Copper Chaperone (COX10) Antibody
COX11, Cytochrome C Oxidase Copper Chaperone (COX10) Antibody, Abbexa, abx322492
COX10 Antibody is a Rabbit Polyclonal against COX10.
Host
Rabbit
Reactivity
Human, Mouse
Applications
ELISA, WB, IHC
Conjugation
Unconjugated
COX11, Cytochrome C Oxidase Copper Chaperone (COX10) Antibody, Abbexa, abx231891
COX10 Antibody is a Rabbit Polyclonal against COX10.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Applications
ELISA, WB
Conjugation
Unconjugated
COX11, Cytochrome C Oxidase Copper Chaperone (COX10) Antibody, Abbexa, abx145373
COX10 Antibody is a Rabbit Polyclonal against COX10.
Host
Rabbit
Reactivity
Human
Applications
ELISA, WB
Conjugation
Unconjugated
COX11, Cytochrome C Oxidase Copper Chaperone (COX10) Antibody, Abbexa, abx111808
Cox10 Homolog, Cytochrome C Oxidase Assembly Protein, Heme A: Farnesyltransferase (Yeast) Antibody is a Rabbit Polyclonal antibody against Cox10 Homolog, Cytochrome C Oxidase Assembly Protein, Heme A: Farnesyltransferase (Yeast).
Host
Rabbit
Reactivity
Human, Mouse, Rat
Applications
ELISA
Conjugation
Unconjugated
COX11, Cytochrome C Oxidase Copper Chaperone (COX10) Antibody, Abbexa, abx025867
Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes heme A:farnesyltransferase, which is not a structural subunit but required for the expression of functional COX and functions in the maturation of the heme A prosthetic group of COX. This protein is predicted to contain 7-9 transmembrane domains localized in the mitochondrial inner membrane. A gene mutation, which results in the substitution of a lysine for an asparagine (N204K), is identified to be responsible for cytochrome c oxidase deficiency. In addition, this gene is disrupted in patients with CMT1A (Charcot-Marie-Tooth type 1A) duplication and with HNPP (hereditary neuropathy with liability to pressure palsies) deletion.
Host
Rabbit
Reactivity
Human
Applications
ELISA, WB, IHC, FCM
Conjugation
Unconjugated
COX11, Cytochrome C Oxidase Copper Chaperone (COX10) Antibody, Abbexa, abx323371
COX10 Antibody is a Rabbit Polyclonal against COX10.
Host
Rabbit
Reactivity
Human
Applications
ELISA, WB
Conjugation
Unconjugated
COX11, Cytochrome C Oxidase Copper Chaperone (COX10) Antibody, Abbexa, abx211427
COX10 Antibody is a Rabbit Polyclonal against COX10.
Host
Rabbit
Reactivity
Human
Applications
ELISA, IHC
Conjugation
Unconjugated
COX11, Cytochrome C Oxidase Copper Chaperone (COX10) Antibody, Abbexa, abx321009
COX10 Antibody is a Rabbit Polyclonal against COX10.
Host
Rabbit
Reactivity
Human
Applications
ELISA, IHC
Conjugation
Unconjugated
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