Collagen, Type IV, alpha 6 (COL4a6) (Middle Region) Peptide
COL4a6
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all COL4a6 products
- COL4a6 (Collagen, Type IV, alpha 6 (COL4a6))
- Protein Region
- Middle Region
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Sequence
- GIKGKSGLPG APGFPGISGH PGKKGTRGKK GPPGSIVKKG LPGLKGLPGN
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-COL4A6 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- COL4a6 (Collagen, Type IV, alpha 6 (COL4a6))
- Synonyms
- CXDELq22.3 Peptide, DELXq22.3 Peptide, BB116301 Peptide, collagen type IV alpha 6 chain Peptide, collagen, type IV, alpha 6 Peptide, COL4A6 Peptide, Col4a6 Peptide, col4a6 Peptide
- Background
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This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. 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, alpha 5 type IV collagen, so that the gene pair shares a common promoter. Deletions in the alpha 5 gene that extend into the alpha 6 gene result in diffuse leiomyomatosis accompanying the X-linked Alport syndrome caused by the deletion in the alpha 5 gene. Two splice variants have been identified for this gene.
Alias Symbols: MGC88184, DELXq22.3, CXDELq22.3
Protein Interaction Partner: APP,CD93,DCN,FBLN2,FN1,HABP2,MATN2,MMP9,OSM,SERPINE2
Protein Size: 1691 - Molecular Weight
- 161 kDa
- Gene ID
- 1288
- NCBI Accession
- NM_001847, NP_001838
- UniProt
- Q14031
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