Transglutaminase 1, Keratinocyte (TGM1) (N-Term) Peptide
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- Target See all TGM1 products
- TGM1 (Transglutaminase 1, Keratinocyte (TGM1))
- Protein Region
- N-Term
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-TGM1 antibody (Catalog #: ARP41713_P050). 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
- TGM1 (Transglutaminase 1, Keratinocyte (TGM1))
- Synonyms
- TGM1 Peptide, ARCI1 Peptide, ICR2 Peptide, KTG Peptide, LI Peptide, LI1 Peptide, TGASE Peptide, TGK Peptide, 2310004J08Rik Peptide, Tgase1 Peptide, transglutaminase 1 Peptide, transglutaminase 1, K polypeptide Peptide, Tgm1 Peptide, TGM1 Peptide
- Background
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TGM1 is a membrane protein that catalyzes the addition of an alkyl group from an akylamine to a glutamine residue of a protein, forming an alkylglutamine in the protein. This protein alkylation leads to crosslinking of proteins and catenation of polyamines to proteins. This gene contains either one or two copies of a 22 nt repeat unit in its 3' UTR. Mutations in this gene have been associated with autosomal recessive lamellar ichthyosis (LI) and nonbullous congenital ichthyosiform erythroderma (NCIE).The protein encoded by this gene is a membrane protein that catalyzes the addition of an alkyl group from an akylamine to a glutamine residue of a protein, forming an alkylglutamine in the protein. This protein alkylation leads to crosslinking of proteins and catenation of polyamines to proteins. This gene contains either one or two copies of a 22 nt repeat unit in its 3' UTR. Mutations in this gene have been associated with autosomal recessive lamellar ichthyosis (LI) and nonbullous congenital ichthyosiform erythroderma (NCIE). Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: ICR2, KTG, LI, LI1, TGASE, TGK
Protein Interaction Partner: RARRES3,HSPB1,MDK,RARRES3,SEMG1,SEMG2
Protein Size: 817 - Molecular Weight
- 90 kDa
- Gene ID
- 7051
- NCBI Accession
- NM_000359, NP_000350
- UniProt
- P22735
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