COX10 Antibody

Product: Fendiline (hydrochloride)

COX10 Antibody Summary

Immunogen
This antibody was developed against Recombinant Protein corresponding to amino acids:CVGGSVWYLERRTIQDSPHKFLHLLRNVNKQWITFQHFSFLKRMYVTQLNRSHNQQVRPKPEPVASPFLEKTSSGQAKAEIYEMRP
Specificity
Specificity of antibody verified on a Protein Array containing target protein plus 383 other non-specific proteins.
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
COX10
Purity
Immunogen affinity purified
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Applications/Dilutions

Dilutions
  • Western Blot 1:100 – 1:250
  • Immunohistochemistry
  • Immunohistochemistry-Paraffin 1:50 – 1:200
Application Notes
For HIER pH6 retrieval is recommended.
Control Peptide
COX10 Protein (NBP1-86322PEP)

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
PBS (pH 7.2) and 40% Glycerol
Preservative
0.02% Sodium Azide
Purity
Immunogen affinity purified

Alternate Names for COX10 Antibody

  • COX10 (yeast) homolog, cytochrome c oxidase assembly protein (heme A:farnesyltransferase)
  • COX10 homolog, cytochrome c oxidase assembly protein, heme A:farnesyltransferase (yeast)
  • cytochrome c oxidase assembly protein
  • cytochrome c oxidase subunit X
  • EC 2.5.1.-
  • heme A: farnesyltransferase
  • Heme O synthase
  • protoheme IX farnesyltransferase, mitochondrial

PMID: 17135407

COX10 Antibody

Product: PSI-7976

COX10 Antibody Summary

Immunogen
This antibody was developed against Recombinant Protein corresponding to amino acids:PNEKELIELEPDSVIEDSIDVGKETKEEKRWKEMKLQVYDLPGILARLS
Specificity
Specificity of antibody verified on a Protein Array containing target protein plus 383 other non-specific proteins.
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
COX10
Purity
Immunogen affinity purified
Innovators Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Learn about the Innovators Reward

Applications/Dilutions

Dilutions
  • Western Blot 1:100 – 1:250
  • Immunohistochemistry
  • Immunohistochemistry-Paraffin 1:200 – 1:500
Application Notes
For HIER pH6 retrieval is recommended.
Control Peptide
COX10 Protein (NBP1-86323PEP)

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
PBS (pH 7.2) and 40% Glycerol
Preservative
0.02% Sodium Azide
Purity
Immunogen affinity purified

Alternate Names for COX10 Antibody

  • COX10 (yeast) homolog, cytochrome c oxidase assembly protein (heme A:farnesyltransferase)
  • COX10 homolog, cytochrome c oxidase assembly protein, heme A:farnesyltransferase (yeast)
  • cytochrome c oxidase assembly protein
  • cytochrome c oxidase subunit X
  • EC 2.5.1.-
  • heme A: farnesyltransferase
  • Heme O synthase
  • protoheme IX farnesyltransferase, mitochondrial

PMID: 12037567

COX10 Antibody

Product: EGF818 (mesylate)

COX10 Antibody Summary

Immunogen
Synthetic peptides corresponding to COX10(COX10 homolog, cytochrome c oxidase assembly protein, heme A) The peptide sequence was selected from the middle region of COX10. Peptide sequence APGPFDWPCFLLTSVGTGLASCAANSINQFFEVPFDSNMNRTKNRPLVRG.
Clonality
Polyclonal
Host
Rabbit
Gene
COX10
Purity
Immunogen affinity purified
Innovators Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Learn about the Innovators Reward

Applications/Dilutions

Dilutions
  • Western Blot 1:100-1:2000
Application Notes
This is a rabbit polyclonal antibody against COX10 and was validated on Western blot.

Packaging, Storage & Formulations

Storage
Store at -20C. Avoid freeze-thaw cycles.
Buffer
PBS and 2% Sucrose
Preservative
0.09% Sodium Azide
Purity
Immunogen affinity purified

Notes

The addition of 50% glycerol is optional for those storing this antibody at -20C and not aliquoting smaller units. However, please note that glycerol may interrupt some downstream antibody applications and should be added with caution.

Alternate Names for COX10 Antibody

  • COX10 (yeast) homolog, cytochrome c oxidase assembly protein (heme A:farnesyltransferase)
  • COX10 homolog, cytochrome c oxidase assembly protein, heme A:farnesyltransferase (yeast)
  • cytochrome c oxidase assembly protein
  • cytochrome c oxidase subunit X
  • EC 2.5.1.-
  • heme A: farnesyltransferase
  • Heme O synthase
  • protoheme IX farnesyltransferase, mitochondrial

Background

Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. COX10 is 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.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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

PMID: 18587423