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Collagen Type VI Alpha 2 (COL6A2) Antibody – Rabbit Polyclonal

For Research Use Only. Not for use in diagnostic procedures. Catalog #: MBS839870

Rabbit polyclonal Collagen Type VI Alpha 2 antibody raised against the C terminal of COL6A2 More details

$990 / 0.1 mL +1 FREE 8GB USB
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

Online Datasheet in PDF
Product Name
Collagen Type VI Alpha 2 (COL6A2), Polyclonal Antibody
Full Product Name
Collagen Type VI Alpha 2 antibody
Product Gene Name
Product Synonym Names
Polyclonal Collagen Type VI Alpha 2; Anti-Collagen Type VI Alpha 2; PP3610; DKFZp586E1322; COL6A2
Clonality
Polyclonal
Host
Rabbit
Form/Format
Lyophilized powder. Add 100ul distilled water for a 1mg/ml concentration of COL6A2 antibody in PBS
Purity/Purification
Total IgG Protein A purified
Concentration
1 mg/ml (lot specific)
Specificity
Collagen Type VI Alpha 2 antibody was raised against the C terminal of COL6A2
Preparation and Storage
Store at 2-8 degree C for short periods. For longer periods of storage, store at -20 degree C. Avoid repeat freeze-thaw cycles.
Molecular Weight
46 kDa (MW of target protein)
OMIM
120240
Cross-Reactivity
Human
Immunogen
Collagen Type VI Alpha 2 antibody was raised using the C terminal of COL6A2 corresponding to a region with amino acids ARRFVEQVARRLTLARRDDDPLNARVALLQFGGPGEQQVAFPLSHNLTAI
Applications Tested/Suitable for anti-COL6A2 antibody
Western Blot (WB)
Application Notes for anti-COL6A2 antibody
WB: 1.25 ug/ml

Western Blot (WB) of anti-COL6A2 antibody

Collagen Type VI Alpha 2 antibody (MBS839870) used at 1.25 ug/ml to detect target protein.
Rabbit Anti-COL6A2 Polyclonal Antibody – Cat# MBS839870

Other Notes

Small volumes of anti-COL6A2 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.

Searchable Terms for COL6A2 purchase

MBS839870 is an antibody targeting COL6A2. Also known as Collagen Type VI Alpha 2 antibody. Host: Rabbit.

Additional Details

NCBI/Uniprot data below describe general gene information for COL6A2. It may not necessarily be applicable to this product.

NCBI GI #
NCBI GeneID
NCBI Accession #
UniProt Secondary Accession #
UniProt Related Accession #
NCBI Official Full Name
Collagen, type VI, alpha 2
NCBI Official Synonym Full Names
collagen, type VI, alpha 2
NCBI Official Symbol
COL6A2
NCBI Official Synonym Symbols
PP3610
UniProt Protein Name
Collagen alpha-2(VI) chain
Protein Family
UniProt Gene Name
COL6A2
UniProt Entry Name
CO6A2_HUMAN
NCBI Protein Information
collagen alpha-2(VI) chain

NCBI Summary for COL6A2

This gene encodes one of the three alpha chains of type VI collagen, a beaded filament collagen found in most connective tissues. The product of this gene contains several domains similar to von Willebrand Factor type A domains. These domains have been shown to bind extracellular matrix proteins, an interaction that explains the importance of this collagen in organizing matrix components. Mutations in this gene are associated with Bethlem myopathy and Ullrich scleroatonic muscular dystrophy. Three transcript variants have been identified for this gene. [provided by RefSeq, Jul 2008]
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UniProt Comments for COL6A2

COL6A2: Collagen VI acts as a cell-binding protein. Defects in COL6A2 are a cause of Bethlem myopathy (BM). BM is a rare autosomal dominant proximal myopathy characterized by early childhood onset (complete penetrance by the age of 5) and joint contractures most frequently affecting the elbows and ankles. Defects in COL6A2 are a cause of Ullrich congenital muscular dystrophy (UCMD); also known as Ullrich scleroatonic muscular dystrophy. UCMD is an autosomal recessive congenital myopathy characterized by muscle weakness and multiple joint contractures, generally noted at birth or early infancy. The clinical course is more severe than in Bethlem myopathy. Defects in COL6A2 are the cause of myosclerosis autosomal recessive (MYOSAR); also known as myosclerotic myopathy or congenital myosclerosis of Lowenthal. A condition characterized by chronic inflammation of skeletal muscle with hyperplasia of the interstitial connective tissue. The clinical picture includes slender muscles with firm 'woody' consistency and restriction of movement of many joints because of muscle contractures. Belongs to the type VI collagen family. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Secreted; Extracellular matrix; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 21q22.3

Cellular Component: extracellular matrix; proteinaceous extracellular matrix; extracellular space; protein complex; collagen; endoplasmic reticulum lumen; extracellular region; vesicle; sarcolemma

Molecular Function: protein binding

Biological Process: axon guidance; extracellular matrix disassembly; collagen catabolic process; extracellular matrix organization and biogenesis; response to glucose stimulus; cell adhesion

Disease: Bethlem Myopathy; Myosclerosis, Autosomal Recessive; Ullrich Congenital Muscular Dystrophy
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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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