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COL7A1

  • Official Full Name

    collagen, type VII, alpha 1

  • Overview

    This gene encodes the alpha chain of type VII collagen. The type VII collagen fibril, composed of three identical alpha collagen chains, is restricted to the basement zone beneath stratified squamous epithelia. It functions as an anchoring fibril between the external epithelia and the underlying stroma. Mutations in this gene are associated with all forms of dystrophic epidermolysis bullosa. In the absence of mutations, however, an acquired form of this disease can result from an autoimmune response made to type VII collagen.
  • Synonyms

    COL7A1; collagen, type VII, alpha 1; EBD1, EBDCT, EBR1, epidermolysis bullosa, dystrophic, dominant and recessive; collagen alpha-1(VII) chain; collagen VII; alpha 1 polypeptide; LC collagen; long-chain collagen; collagen VII, alpha-1 polypeptide; EBD1;

  • Recombinant Proteins
  • Protein Pre-coupled Magnetic Beads
  • Human
  • Mouse
  • E.coli
  • HEK293
  • HEK293T
  • Mammalian Cell
  • Mammalian cells
  • Flag
  • His
  • His (Fc)
  • Avi
  • Myc
  • DDK
Species Cat.# Product name Source (Host) Tag Protein Length Price
Human COL7A1-1006HFL Recombinant Full Length Human COL7A1 Protein, C-Flag-tagged Mammalian cells Flag
Human COL7A1-340H Recombinant Human COL7A1 Protein, His-tagged E.coli His Pro190~Asp472
Human COL7A1-638H Recombinant Human COL7A1 Protein, His (Fc)-Avi-tagged HEK293 His (Fc)-Avi
Human COL7A1-30HL Recombinant Human COL7A1 Cell Lysate, Myc/DDK-tagged HEK293T Myc/DDK
Human COL7A1-341H Recombinant Human COL7A1 Protein, Myc/DDK-tagged HEK293T Myc/DDK
Human COL7A1-638H-B Recombinant Human COL7A1 Protein Pre-coupled Magnetic Beads HEK293
Mouse COL7A1-3751M Recombinant Mouse COL7A1 Protein Mammalian Cell His
Mouse COL7A1-1872M-B Recombinant Mouse COL7A1 Protein Pre-coupled Magnetic Beads HEK293
Mouse COL7A1-1872M Recombinant Mouse COL7A1 Protein, His (Fc)-Avi-tagged HEK293 His (Fc)-Avi
  • Involved Pathway
  • Protein Function
  • Interacting Protein
  • COL7A1 Related Articles

COL7A1 involved in several pathways and played different roles in them. We selected most pathways COL7A1 participated on our site, such as Protein digestion and absorption, which may be useful for your reference. Also, other proteins which involved in the same pathway with COL7A1 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

Pathway Name Pathway Related Protein
Protein digestion and absorptionSLC3A1;COL7A1;CELA2B;ATP1A4;PGA4;ATP1B2;COL6A4;PRSS3;CPA1

COL7A1 has several biochemical functions, for example, identical protein binding, peptidase inhibitor activity, serine-type endopeptidase inhibitor activity. Some of the functions are cooperated with other proteins, some of the functions could acted by COL7A1 itself. We selected most functions COL7A1 had, and list some proteins which have the same functions with COL7A1. You can find most of the proteins on our site.

Function Related Protein
identical protein bindingPRKAB2;SH3GLB1;CRYAA;KCNIP2;CLDN8;PARK7;OAT;SP100;PNMA5
peptidase inhibitor activityPI15A;COL7A1;SERPINB10;SERPINA3K;MUG1;SSPO;PI15;SERPINA1A;PTTG1
serine-type endopeptidase inhibitor activityWFDC6B;SERPINA5;SERPINB1L2;APPB;SPINT4;SERPINA1D;PAPLNB;SPINK13;SERPINC1

COL7A1 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with COL7A1 here. Most of them are supplied by our site. Hope this information will be useful for your research of COL7A1.

Ywhae

Tampoia, M; Bonamonte, D; et al. Prevalence of specific anti-skin autoantibodies in a cohort of patients with inherited epidermolysis bullosa. ORPHANET JOURNAL OF RARE DISEASES 8:-(2013).
Has, C; et al. Molecular genetic assays for inherited epidermolysis bullosa. CLINICS IN DERMATOLOGY 29:420-426(2011).
  • Q&As
  • Reviews

Q&As (6)

Ask a question
How is the COL7A1 gene mutation diagnosed? 08/15/2022

It can be diagnosed through genetic testing and skin biopsies. Genetic testing can detect mutations in the COL7A1 gene, while skin biopsies can observe abnormalities in skin structure.

What are the treatments for COL7A1 gene mutations? 08/26/2021

There is currently no cure for the COL7A1 gene mutation, but there are treatments that can relieve symptoms, such as the use of special dressings, medication, and surgery.

What types of skin damage is COL7A1 associated with? 03/22/2021

The COL7A1 gene has been implicated in a variety of skin injuries, including burns, trauma, and surgical trauma. These injuries may lead to skin complications in DEB patients.

What happens to a mutation in the COL7A1 gene? 10/30/2020

Mutations in the COL7A1 gene can cause structural abnormalities in the skin, making it fragile and prone to blisters and scarring, which can be accompanied by abnormalities in bones and internal organs.

Which drug responses are involved in the COL7A1 gene? 08/01/2020

Certain drugs may have efficacy or side effects on the COL7A1 gene mutation, for example, certain immunosuppressants used to treat other skin conditions may have adverse effects on the skin of DEB patients.

How to improve the COL7A1 gene mutation through diet? 02/12/2020

Although there is no conclusive evidence that diet can improve the COL7A1 gene mutation, maintaining a balanced diet with adequate protein, vitamins and minerals is beneficial for overall health.

Customer Reviews (3)

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Reviews
06/24/2023

    COL7A1 is less polluting, safe and hygienic, and suitable for long-term use.

    02/13/2022

      It is stable under different temperature and pH conditions.

      05/09/2020

        Their service attitude is very good and always patient to answer our questions.

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