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Mouse Anti-COX5A Recombinant Antibody (CBYY-C2072) (CBMAB-C3510-YY)

This product is mouse antibody that recognizes COX5A. The antibody CBYY-C2072 can be used for immunoassay techniques such as: WB, IHC-P, FC, IF
See all COX5A antibodies

Summary

Host Animal
Mouse
Specificity
Mouse, Rat, Cattle, Human, Zebrafish
Clone
CBYY-C2072
Antibody Isotype
IgG2a
Application
WB, IHC-P, FC, IF

Basic Information

Specificity
Mouse, Rat, Cattle, Human, Zebrafish
Antibody Isotype
IgG2a
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Buffer
1 mg/mL
Concentration
Liquid
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
Cytochrome C Oxidase Subunit 5A
Entrez Gene ID
Human9377
Mouse12858
Rat252934
Cattle444878
Zebrafish554101
UniProt ID
HumanP20674
MouseP12787
RatP11240
CattleP00426
ZebrafishQ4VBU7
Alternative Names
RNA Transcription, Translation And Transport Factor; RLL Motif Containing 1; CLE7 Homolog; C14orf166; HCLE; CLE; RNA Transcription, Translation And Transport Factor Protein; Chromosome 14 Open Reading Frame 166;
Function
Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane transport and the ATP synthase. Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Electrons originating from reduced cytochrome c in the intermembrane space (IMS) are transferred via the dinuclear copper A center (CU(A)) of subunit 2 and heme A of subunit 1 to the active site in subunit 1, a binuclear center (BNC) formed by heme A3 and copper B (CU(B)). The BNC reduces molecular oxygen to 2 water molecules using 4 electrons from cytochrome c in the IMS and 4 protons from the mitochondrial matrix.
Biological Process
Mitochondrial electron transport, cytochrome c to oxygen Source: GO_Central
Cellular Location
Mitochondrion inner membrane
Involvement in disease
Mitochondrial complex IV deficiency, nuclear type 20 (MC4DN20):
An autosomal recessive mitochondrial disorder with onset in early infancy. MC4DN20 is characterized by pulmonary arterial hypertension, poor feeding, failure to thrive, hypotonia, delayed development, increased serum lactate and metabolic acidosis. Death in infancy occurs due to cardiorespiratory failure. Patient tissues show variably decreased levels and activity of mitochondrial respiratory complex IV.

Zeng, J., Li, G., Xia, Y., Wang, F., Wang, Y., Xu, S., ... & Zhang, J. (2020). miR-204/COX5A axis contributes to invasion and chemotherapy resistance in estrogen receptor-positive breast cancers. Cancer Letters, 492, 185-196.

Xiyang, Y. B., Liu, R., Wang, X. Y., Li, S., Zhao, Y., Lu, B. T., ... & Zhang, J. (2020). COX5A plays a vital role in memory impairment associated with brain aging via the BDNF/ERK1/2 signaling pathway. Frontiers in aging neuroscience, 12, 215.

Jiang, Y., Bai, X., Li, T. T., Al-Hawwas, M., Jin, Y., Zou, Y., ... & Xiong, L. L. (2020). COX5A over-expression protects cortical neurons from hypoxic ischemic injury in neonatal rats associated with TPI up-regulation. BMC neuroscience, 21(1), 1-15.

Zhang, P., Chen, Z., Lu, D., Wu, Y., Fan, M., Qian, J., & Ge, J. (2020). Overexpression of COX5A protects H9c2 cells against doxorubicin-induced cardiotoxicity. Biochemical and Biophysical Research Communications, 524(1), 43-49.

Huang, Y., Li, S. N., Zhou, X. Y., Zhang, L. X., Chen, G. X., Wang, T. H., ... & Zhang, X. (2019). The dual role of AQP4 in cytotoxic and vasogenic edema following spinal cord contusion and its possible association with energy metabolism via COX5A. Frontiers in Neuroscience, 584.

Baertling, F., Al‐Murshedi, F., Sánchez‐Caballero, L., Al‐Senaidi, K., Joshi, N. P., Venselaar, H., ... & Rodenburg, R. J. (2017). Mutation in mitochondrial complex IV subunit COX5A causes pulmonary arterial hypertension, lactic acidemia, and failure to thrive. Human mutation, 38(6), 692-703.

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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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