phospholipase C, beta 1 (phosphoinositide-Specific) (PLCB1) Peptide
PLCB1
Reactivité: Humain
Hôte: Synthetic
BP, WB
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- Antigène Tous les produits Phospholipase C beta 1 (PLCB1)
- Phospholipase C beta 1 (PLCB1) (phospholipase C, beta 1 (phosphoinositide-Specific) (PLCB1))
- Origine
- Humain
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-PLCB antibody (Catalog #: ARP74371_P050) made by Aviva Systems Biology. 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.
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- Indications d'application
- Optimal working dilution should be determined by the investigator.
- 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.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- Phospholipase C beta 1 (PLCB1) (phospholipase C, beta 1 (phosphoinositide-Specific) (PLCB1))
- Synonymes
- PLCB1 Peptide, 3110043I21Rik Peptide, AI132408 Peptide, Plcb Peptide, mKIAA0581 Peptide, EIEE12 Peptide, PI-PLC Peptide, PLC-154 Peptide, PLC-I Peptide, PLC154 Peptide, PLCB1A Peptide, PLCB1B Peptide, PLC'1 Peptide, PLCbeta1 Peptide, Phosphb Peptide, RATPHOSPHB Peptide, phospholipase C beta 1 Peptide, phospholipase C beta 1 S homeolog Peptide, phospholipase C, beta 1 Peptide, PLCB1 Peptide, plcb1.S Peptide, Plcb1 Peptide
- Sujet
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This gene encodes a member of the 1-acylglycerol-3-phosphate O-acyltransferase family. The protein is located within the endoplasmic reticulum membrane and converts lysophosphatidic acid to phosphatidic acid, the second step in de novo phospholipid biosynthesis. Mutations in this gene have been associated with congenital generalized lipodystrophy (CGL), or Berardinelli-Seip syndrome, a disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
Protein Size: 278 - Poids moléculaire
- 30 kDa
- ID gène
- 10555
- NCBI Accession
- NP_006403
- UniProt
- O15120
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