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COX7B Antibody – Rabbit Polyclonal

For Research Use Only. Not for use in diagnostic procedures. Catalog #: MBS768141

MBS768141 is an antibody targeting COX7B. Also known as COX7B Rabbit Polyclonal. Reactive in Human. Host: Rabbit. More details

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Product Documentation
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Sample Manual Insert View PDF
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Testing Data View PDF
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Certificate of Analysis (COA) View PDF
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QC Report View PDF
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Material Safety Data Sheet View PDF
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Technical Datasheet View PDF
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Protocol View PDF

Product Overview

Product Name
COX7B, Polyclonal Antibody
Full Product Name
COX7B Rabbit Polyclonal
Product Gene Name
Clonality
Polyclonal
Isotype
IgG
Host
Rabbit
Species Reactivity
Human
Form/Format
Liquid
Purity/Purification
>=95% as determined by SDS-PAGE
Immunogen Affinity Purified
Preparation and Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20 degree C for 24 months (Avoid repeated freeze / thaw cycles.)
Molecular Weight
9,161 Da
OMIM
300885
Immunogen
Cytochrome c oxidase subunit VIIb
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Applications Tested/Suitable for anti-COX7B antibody
ELISA (EIA), Immunohistochemistry (IHC), Western Blot (WB)

Immunohistochemistry (IHC) of anti-COX7B antibody

Immunohistochemistry of paraffin-embedded human lymphoma using MBS768141 (COX7B antibody) at dilution of 1:100
Rabbit Anti-COX7B Polyclonal Antibody – Cat# MBS768141

Western Blot (WB) of anti-COX7B antibody

human skeletal muscle tissue were subjected to SDS PAGE followed by western blot with MBS768141 (COX7B antibody) at dilution of 1:400
Rabbit Anti-COX7B Polyclonal Antibody, Western Blot (WB) – Cat# MBS768141

Other Notes

Small volumes of anti-COX7B antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

Additional Details

NCBI/Uniprot data below describe general gene information for COX7B. It may not necessarily be applicable to this product.

NCBI GI #
NCBI GeneID
NCBI Accession #
UniProt Secondary Accession #
UniProt Related Accession #
GenBank Nucleotide #
NCBI Official Full Name
cytochrome c oxidase subunit 7B, mitochondrial
NCBI Official Synonym Full Names
cytochrome c oxidase subunit 7B
NCBI Official Symbol
COX7B
NCBI Official Synonym Symbols
APLCC; LSDMCA2
UniProt Protein Name
Cytochrome c oxidase subunit 7B, mitochondrial
UniProt Synonym Protein Names
Cytochrome c oxidase polypeptide VIIb
Protein Family
UniProt Gene Name
COX7B
UniProt Entry Name
COX7B_HUMAN
NCBI Protein Information
cytochrome c oxidase subunit 7B, mitochondrial

NCBI Summary for COX7B

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 subunit VIIb, which is highly similar to bovine COX VIIb protein and is found in all tissues. This gene may have several pseudogenes on chromosomes 1, 2, 20 and 22. [provided by RefSeq, Jun 2011]
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UniProt Comments for COX7B

COX7B: This protein is one of the nuclear-coded polypeptide chains of cytochrome c oxidase, the terminal oxidase in mitochondrial electron transport. Belongs to the cytochrome c oxidase VIIb family.

Protein type: Membrane protein, integral; Mitochondrial; Oxidoreductase

Chromosomal Location of Human Ortholog: Xq21.1

Cellular Component: integral to membrane; mitochondrial inner membrane; mitochondrial respiratory chain; mitochondrion

Molecular Function: cytochrome-c oxidase activity

Biological Process: central nervous system development; mitochondrial electron transport, cytochrome c to oxygen

Disease: Aplasia Cutis Congenita, Reticulolinear, With Microcephaly, Facial Dysmorphism, And Other Congenital Anomalies
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Precautions

All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.

Disclaimer

While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.

Product Note

Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual, it is intended to serve as an example only. Please refer to the instructions For Use provided with the assay kit for precise details.

Product PubMed Publications

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