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Recombinant Human Collagen I protein is a Human Fragment protein, in the 1021 to 1108 aa range, expressed in Wheat germ and suitable for SDS-PAGE, ELISA, WB.

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SDS-PAGE - Recombinant Human Collagen I protein (AB158152), expandable thumbnail

Publications

Key facts

Expression system
Wheat germ
Tags
GST tag N-Terminus
Applications
SDS-PAGE, ELISA, WB
Biologically active
No

Amino acid sequence

E G S P G R D G S P G A K G D R G E T G P A G P P G A P G A P G A P G P V G P A G K S G D R G E T G P A G P A G P V G P V G A R G P A G P Q G P R G D K G E T G E Q G D R G I K

Reactivity data

Application
SDS-PAGE
Reactivity
Reacts
Dilution info
-
Notes

-

Application
ELISA
Reactivity
Reacts
Dilution info
-
Notes

-

Application
WB
Reactivity
Reacts
Dilution info
-
Notes

-

Associated Products

Select an associated product type

2 products for Alternative Product

Target data

Function

Type I collagen is a member of group I collagen (fibrillar forming collagen).

Alternative names

Recommended products

Recombinant Human Collagen I protein is a Human Fragment protein, in the 1021 to 1108 aa range, expressed in Wheat germ and suitable for SDS-PAGE, ELISA, WB.

Key facts

Expression system
Wheat germ
Applications
SDS-PAGE, ELISA, WB
Accession
P02452-1
Animal free
No
Species
Human
Concentration
Loading...
Storage buffer

pH: 8
Constituents: 0.79% Tris HCl, 0.31% Glutathione

Sequence info

Amino acid sequence

E G S P G R D G S P G A K G D R G E T G P A G P P G A P G A P G A P G P V G P A G K S G D R G E T G P A G P A G P V G P V G A R G P A G P Q G P R G D K G E T G E Q G D R G I K
Accession
P02452
Protein length
Fragment
Predicted molecular weight
35.42 kDa
Amino acids
1021 to 1108
Nature
Recombinant
Tags
GST tag N-Terminus

Specifications

Form
Liquid
Additional notes

Glutathione Sepharose 4 Fast Flow

General info

Function

Type I collagen is a member of group I collagen (fibrillar forming collagen).

Sequence similarities

Belongs to the fibrillar collagen family.

Post-translational modifications

Contains mostly 4-hydroxyproline. Proline residues at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains.

Storage

Shipped at conditions
Dry Ice
Appropriate short-term storage conditions
-80°C
Appropriate long-term storage conditions
-80°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary info

This supplementary information is collated from multiple sources and compiled automatically.
Activity summary

Collagen type I also called collagen I is a structural protein expressed mainly in connective tissues such as skin tendon bone and ligaments. It serves as an important component in providing mechanical strength and integrity to these tissues. Collagen I is a fibrillar collagen known for its triple-helix structure composed of two alpha-1 chains and one alpha-2 chain and has a molecular mass of approximately 300 kDa. Researchers often employ collagen western blot and collagen ELISA techniques for its detection. Collagen suppliers offer various collagen antibodies used in these assays to study its distribution and function.

Biological function summary

Collagen type I plays a central role in maintaining the extracellular matrix and supporting cellular environments. It interacts with other matrix proteins and cells forming complexes that help in tissue development and repair. Type I collagen is especially important in bone matrix working alongside minerals like hydroxyapatite to provide rigidity and support. Anti-collagen antibodies aid in studying its biological functions and interactions which are critical to understanding tissue dynamics.

Pathways

Collagen type I interacts with multiple signaling cascades involved in tissue remodeling and repair. It is a significant player in the TGF-β pathway which regulates fibrosis and wound healing processes. In these pathways proteins such as fibronectin and integrins work in concert with collagen type I to orchestrate cellular responses to damage. Researchers often examine its role in these pathways to uncover therapeutic possibilities for disease interventions.

Associated diseases and disorders

Collagen type I has strong connections to conditions like osteogenesis imperfecta and fibrosis. Mutations or irregularities in collagen I production can lead to osteogenesis imperfecta a genetic disorder characterized by brittle bones. In fibrosis excessive collagen deposition disrupts normal tissue architecture contributing to organ dysfunction. In both conditions type I collagen interacts with other proteins like matrix metalloproteinases which modulate its breakdown and remodeling highlighting its importance in disease pathology.

Product promise

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In the unlikely event of one of our products not working as expected, you are covered by our product promise.

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1 product image

  • SDS-PAGE - Recombinant Human Collagen I protein (ab158152), expandable thumbnail

    SDS-PAGE - Recombinant Human Collagen I protein (ab158152)

    ab158152 on a 12.5% SDS-PAGE stained with Coomassie Blue.

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Product protocols

For this product, it's our understanding that no specific protocols are required. You can:

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