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COL5A1, Blocking Peptide

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產(chǎn)品名稱: COL5A1, Blocking Peptide
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COL5A1, Blocking Peptide


COL5A1, Blocking Peptide  的詳細(xì)介紹
Product Name

COL5A1, Blocking Peptide

Full Product Name

COL5A1 Antibody (N-term) Blocking Peptide

Product Synonym Names
Collagen alpha-1(V) chain; COL5A1
Product Gene Name

COL5A1 blocking peptide

[Similar Products]
Antibody/Peptide Pairs
COL5A1 peptide (MBS9217625) is used for blocking the activity of COL5A1 antibody (MBS9209492)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
120215
3D Structure
ModBase 3D Structure for P20908
Form/Format
Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.
Cellular Location
Secreted, extracellular space, extracellular matrix
Preparation and Storage
Maintain refrigerated at 2-8 degree C for up to 6 months. For long term storage store at -20 degree C.
Other Notes
Small volumes of COL5A1 blocking peptide 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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Related Product Information for
COL5A1 blocking peptide
Type V collagen is a member of group I collagen (fibrillar forming collagen). It is a minor connective tissue component of nearly ubiquitous distribution. Type V collagen binds to DNA, heparan sulfate, thrombospondin, heparin, and insulin.
NCBI/Uniprot data below describe general gene information for COL5A1. It may not necessarily be applicable to this product.
NCBI GI #
89276751
NCBI GeneID
1289
NCBI Accession #
NP_000084.3 [Other Products]
NCBI GenBank Nucleotide #
NM_000093.4 [Other Products]
UniProt Primary Accession #
P20908 [Other Products]
UniProt Secondary Accession #
Q15094; Q5SUX4[Other Products]
UniProt Related Accession #
P20908[Other Products]
Molecular Weight
183,560 Da
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NCBI Official Full Name
collagen alpha-1(V) chain isoform 1 preproprotein
NCBI Official Synonym Full Names
collagen type V alpha 1 chain
NCBI Official Symbol
COL5A1??[Similar Products]
NCBI Official Synonym Symbols
EDSC
??[Similar Products]
NCBI Protein Information
collagen alpha-1(V) chain
UniProt Protein Name
Collagen alpha-1(V) chain
Protein Family
Collagen
UniProt Gene Name
COL5A1??[Similar Products]
UniProt Entry Name
CO5A1_HUMAN
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NCBI Summary for COL5A1
This gene encodes an alpha chain for one of the low abundance fibrillar collagens. Fibrillar collagen molecules are trimers that can be composed of one or more types of alpha chains. Type V collagen is found in tissues containing type I collagen and appears to regulate the assembly of heterotypic fibers composed of both type I and type V collagen. This gene product is closely related to type XI collagen and it is possible that the collagen chains of types V and XI constitute a single collagen type with tissue-specific chain combinations. The encoded procollagen protein occurs commonly as the heterotrimer pro-alpha1(V)-pro-alpha1(V)-pro-alpha2(V). Mutations in this gene are associated with Ehlers-Danlos syndrome, types I and II. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]
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UniProt Comments for COL5A1
COL5A1: Type V collagen is a member of group I collagen (fibrillar forming collagen). It is a minor connective tissue component of nearly ubiquitous distribution. Type V collagen binds to DNA, heparan sulfate, thrombospondin, heparin, and insulin. Defects in COL5A1 are a cause of Ehlers-Danlos syndrome type 1 (EDS1); also known as Ehlers-Danlos syndrome gravis or severe classic type Ehlers-Danlos syndrome. EDS is a connective tissue disorder characterized by hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity. EDS1 is the severe form of classic Ehlers-Danlos syndrome. Defects in COL5A1 are a cause of Ehlers-Danlos syndrome type 2 (EDS2); also known as Ehlers-Danlos syndrome mitis or mild classic type Ehlers Danlos syndrome. Belongs to the fibrillar collagen family.

Protein type: Extracellular matrix; Cell adhesion; Motility/polarity/chemotaxis; Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 9q34.2-q34.3

Cellular Component: collagen type V; endoplasmic reticulum lumen; extracellular matrix; extracellular region

Molecular Function: heparin binding; platelet-derived growth factor binding; proteoglycan binding

Biological Process: cell adhesion; cell migration; collagen biosynthetic process; collagen catabolic process; collagen fibril organization; extracellular matrix organization and biogenesis; eye morphogenesis; fibril organization and biogenesis; integrin biosynthetic process; skin development; wound healing, spreading of epidermal cells

Disease: Ehlers-danlos Syndrome, Type I
Research Articles on COL5A1
1. Data (including data from studies in knockout mice) suggest causative role for collagen(V)alpha1 hypersensitivity/autoimmunity in pathogenesis of atherosclerosis; both immune tolerance and reduction of plaque burden are dependent on interleukin 35.
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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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