FYVE, RhoGEF and PH Domain Containing 1 (FGD1) Peptide
FGD1
Reactivité: Humain
Hôte: Synthetic
BP, WB
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- Antigène Tous les produits FGD1
- FGD1 (FYVE, RhoGEF and PH Domain Containing 1 (FGD1))
- 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-FGD1 antibody (Catalog #: ARP38472_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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- 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
- FGD1 (FYVE, RhoGEF and PH Domain Containing 1 (FGD1))
- Synonymes
- AAS Peptide, FGDY Peptide, MRXS16 Peptide, ZFYVE3 Peptide, FYVE, RhoGEF and PH domain containing 1 Peptide, FGD1 Peptide, Fgd1 Peptide, fgd1 Peptide
- Sujet
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FGD1 contains Dbl (DH) and pleckstrin (PH) homology domains. It can bind specifically to the Rho family GTPase Cdc42Hs and stimulate the GDP-GTP exchange of the isoprenylated form of Cdc42Hs. It also stimulates the mitogen activated protein kinase cascade leading to c-Jun kinase SAPK/JNK1 activation. FGD1 has an essential role in embryonic development, and FGD1 gene mutations result in the human developmental disorder, Aarskog-Scott syndrome.FGD1 contains Dbl (DH) and pleckstrin (PH) homology domains. It can bind specifically to the Rho family GTPase Cdc42Hs and stimulate the GDP-GTP exchange of the isoprenylated form of Cdc42Hs. It also stimulates the mitogen activated protein kinase cascade leading to c-Jun kinase SAPK/JNK1 activation. FGD1 has an essential role in embryonic development, and FGD1 gene mutations result in the human developmental disorder, Aarskog-Scott syndrome. 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: AAS, FGDY, ZFYVE3, MRXS16
Protein Interaction Partner: ABP1,CDC42,CTTN,ELMO1,CDC42
Protein Size: 961 - Poids moléculaire
- 106 kDa
- ID gène
- 2245
- NCBI Accession
- NM_004463, NP_004454
- UniProt
- P98174
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