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Collagen Type IV Protein | COL4A5 protein

Collagen Type IV, Human (Arresten, ASLN, ATS, CA54, Canstatin, COL4A1, COL4A2, Collagen Alpha 1(IV) Chain, Collagen Alpha 2(IV) Chain, Collagen IV Alpha 1 Polypeptide, Collagen IV Alpha 2 Polypeptide, Collagen of Basement Membrane Alpha 1 Chain, Collagen

Gene Names
COL4A5; ATS; ASLN; CA54
Purity
Purified
~90% (SDS-PAGE). Controlled and limited pepsin digestion, followed by selective salt precipitation.
Synonyms
Collagen Type IV; Human (Arresten; ASLN; ATS; CA54; Canstatin; COL4A1; COL4A2; Collagen Alpha 1(IV) Chain; Collagen Alpha 2(IV) Chain; Collagen IV Alpha 1 Polypeptide; Collagen IV Alpha 2 Polypeptide; Collagen of Basement Membrane Alpha 1 Chain; Collagen; COL4A5 protein
Ordering
For Research Use Only!
Host
Placental villi
Purity/Purification
Purified
~90% (SDS-PAGE). Controlled and limited pepsin digestion, followed by selective salt precipitation.
Form/Format
Supplied as a liquid in 500mM acetic acid. No preservative added.
Application Notes
Suitable for use as Type IV collagen standard, antigen for antibody production, coating material for cell culture studies, and formation of collagen gels.
Preparation and Storage
May be stored at 4 degree C for short-term only. For long-term storage, aliquot and store at -20 degree C. Aliquots are stable for at least 6 months at -20 degree C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.
Related Product Information for COL4A5 protein
Collagens are highly conserved throughout evolution and are characterised by an uninterrupted "Glycine X Y" triplet repeat that is a necessary part of the triple helical structure. Type I collagen (95 kDa) is found in bone, cornea, skin and tendon. Mutations in the encoding gene are associated with osteogenesis imperfecta, Ehlers Danlos syndrome, and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for Platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor.
Product Categories/Family for COL4A5 protein

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
UniProt Accession #
Molecular Weight
161,044 Da
NCBI Official Full Name
collagen type IV alpha 5 chain, partial
NCBI Official Synonym Full Names
collagen, type IV, alpha 5
NCBI Official Symbol
COL4A5
NCBI Official Synonym Symbols
ATS; ASLN; CA54
NCBI Protein Information
collagen alpha-5(IV) chain; collagen alpha-5(IV) chain; dA24A23.1; dA149D17.3; collagen IV, alpha-5 polypeptide; collagen of basement membrane, alpha-5 chain
UniProt Protein Name
Collagen alpha-5(IV) chain
Protein Family
UniProt Gene Name
COL4A5
UniProt Entry Name
CO4A5_HUMAN

NCBI Description

This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Mutations in this gene are associated with X-linked Alport syndrome, also known as hereditary nephritis. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Aug 2010]

Uniprot Description

COL4A5: Type IV collagen is the major structural component of glomerular basement membranes (GBM), forming a 'chicken-wire' meshwork together with laminins, proteoglycans and entactin/nidogen. Defects in COL4A5 are the cause of Alport syndrome X- linked (APSX). APSX is characterized by progressive glomerulonephritis, renal failure, sensorineural deafness, specific eye abnormalities (lenticonous and macular flecks), and glomerular basement membrane defects. The disorder shows considerable heterogeneity in that families differ in the age of end-stage renal disease and the occurrence of deafness. Deletions covering the N-terminal regions of COL4A5 and COL4A6, which are localized in a head-to-head manner, are found in the chromosome Xq22.3 centromeric deletion syndrome. This results in a phenotype with features of diffuse leiomyomatosis and Alport syndrome (DL-ATS). Belongs to the type IV collagen family. 2 isoforms of the human protein are produced by alternative splicing.

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

Chromosomal Location of Human Ortholog: Xq22

Cellular Component: endoplasmic reticulum lumen; collagen type IV; extracellular region; basal lamina; neuromuscular junction

Molecular Function: extracellular matrix structural constituent

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

Disease: Alport Syndrome, X-linked

Research Articles on COL4A5

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Product Notes

The COL4A5 col4a5 (Catalog #AAA634449) is a Protein produced from Placental villi and is intended for research purposes only. The product is available for immediate purchase. Suitable for use as Type IV collagen standard, antigen for antibody production, coating material for cell culture studies, and formation of collagen gels. Researchers should empirically determine the suitability of the COL4A5 col4a5 for an application not listed in the data sheet. Researchers commonly develop new applications and it is an integral, important part of the investigative research process. It is sometimes possible for the material contained within the vial of "Collagen Type IV, Protein" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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