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Collagen IX alpha2, Antibody

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產(chǎn)品名稱: Collagen IX alpha2, Antibody
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Collagen IX alpha2, Antibody


Collagen IX alpha2, Antibody  的詳細(xì)介紹
Product Name

Collagen IX alpha2 (COL9A2), Antibody

Full Product Name

Rabbit Collagen IX alpha2 Antibody

Product Synonym Names
Collagen IX a2
Product Gene Name

anti-COL9A2 antibody

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Chromosome Location
Chromosome: 1; NC_000001.10 (40766163..40782939, complement). Location: 1p33-p32
OMIM
120260
3D Structure
ModBase 3D Structure for Q14055
Host
Rabbit
Species Reactivity
Human, mouse
Form/Format
Phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol
Concentration
1 mg/ml (lot specific)
Other Notes
Small volumes of anti-COL9A2 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.
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Applications Tested/Suitable for anti-COL9A2 antibody
ELISA (EIA), Western Blot (WB)
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NCBI/Uniprot data below describe general gene information for COL9A2. It may not necessarily be applicable to this product.
NCBI GI #
11386161
NCBI GeneID
1298
NCBI Accession #
NP_001843.1 [Other Products]
NCBI GenBank Nucleotide #
NM_001852.3 [Other Products]
UniProt Primary Accession #
Q14055 [Other Products]
UniProt Secondary Accession #
B2RMP9[Other Products]
UniProt Related Accession #
Q14055[Other Products]
Molecular Weight
65,131 Da[Similar Products]
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NCBI Official Full Name
collagen alpha-2(IX) chain
NCBI Official Synonym Full Names
collagen, type IX, alpha 2
NCBI Official Symbol
COL9A2??[Similar Products]
NCBI Official Synonym Symbols
MED; EDM2; STL5; DJ39G22.4
??[Similar Products]
NCBI Protein Information
collagen alpha-2(IX) chain; collagen alpha-2(IX) chain; alpha 2 type IX collagen; collagen IX, alpha-2 polypeptide
UniProt Protein Name
Collagen alpha-2(IX) chain
Protein Family
Collagen
UniProt Gene Name
COL9A2??[Similar Products]
UniProt Entry Name
CO9A2_HUMAN
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NCBI Summary for COL9A2
This gene encodes one of the three alpha chains of type IX collagen, the major collagen component of hyaline cartilage. Type IX collagen, a heterotrimeric molecule, is usually found in tissues containing type II collagen, a fibrillar collagen. This chain is unusual in that, unlike the other two type IX alpha chains, it contains a covalently attached glycosaminoglycan side chain. Mutations in this gene are associated with multiple epiphyseal dysplasia. [provided by RefSeq, Jul 2008]
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UniProt Comments for COL9A2
COL9A2: Structural component of hyaline cartilage and vitreous of the eye. Defects in COL9A2 are the cause of multiple epiphyseal dysplasia type 2 (EDM2). EDM is a generalized skeletal dysplasia associated with significant morbidity. Joint pain, joint deformity, waddling gait, and short stature are the main clinical signs and symptoms. EDM is broadly categorized into the more severe Fairbank and the milder Ribbing types. EDM2 inheritance is autosomal dominant. Defects in COL9A2 may be a cause of susceptibility to intervertebral disc disease (IDD); also known as lumbar disk herniation (LDH). IDD is one of the most common musculo-skeletal disorders and the predominant cause of low-back pain and unilateral leg pain. Defects in COL9A2 are the cause of Stickler syndrome type 5 (STL5). An autosomal recessive form of Stickler syndrome, an inherited disorder that associates ocular signs with more or less complete forms of Pierre Robin sequence, bone disorders and sensorineural deafness. STL5 is characterized by high myopia, vitreoretinal degeneration, retinal detachment, mild to moderate sensorineural hearing loss, short stature in childhood, and absence of cleft palate and Pierre Robin sequence. Belongs to the fibril-associated collagens with interrupted helices (FACIT) family.

Protein type: Secreted, signal peptide; Secreted

Chromosomal Location of Human Ortholog: 1p33-p32

Cellular Component: proteinaceous extracellular matrix; endoplasmic reticulum lumen; extracellular region

Molecular Function: extracellular matrix structural constituent conferring tensile strength

Biological Process: axon guidance; extracellular matrix disassembly; collagen catabolic process; extracellular matrix organization and biogenesis; skeletal development

Disease: Intervertebral Disc Disease; Epiphyseal Dysplasia, Multiple, 2; Stickler Syndrome, Type V
Research Articles on COL9A2
1. The NC2 domain of type IX collagen determines the chain composition but also the chain register of the triple helix.
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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.
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