Loricrin (LOR) Peptide
LOR
Reactivité: Humain
Hôte: Synthetic
BP, IHC, WB
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- Antigène Tous les produits LOR
- LOR (Loricrin (LOR))
- Origine
- Humain
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-LOR antibody (Catalog #: ARP41738_T100). 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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- Indications d'application
- 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.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- LOR (Loricrin (LOR))
- Synonymes
- AI036317 Peptide, S77319 Peptide, RGD1559993 Peptide, LOR Peptide, loricrin Peptide, Loricrin Peptide, LOR Peptide, Lor Peptide, TVAG_146950 Peptide, TVAG_228830 Peptide, TVAG_228920 Peptide, TVAG_238290 Peptide, TVAG_035050 Peptide, TVAG_070680 Peptide, Bm1_52290 Peptide, LOC100281109 Peptide, LOC100281170 Peptide
- Classe de substances
- Chemical
- Sujet
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LOR is a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in this gene are associated with Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases.LOR encodes loricrin, a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in LOR may be the cause of both Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases.
Alias Symbols: MGC111513
Protein Interaction Partner: EVPL,SPRR3,VIM,CSTA,IVL,KRT1,LOR,PI3,VIM
Protein Size: 316 - Poids moléculaire
- 35 kDa
- ID gène
- 4014
- NCBI Accession
- NM_000427, NP_000418
- UniProt
- P23490
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