Growth Hormone Receptor (GHR) (N-Term) Peptid
GHR
Reaktivität: Human
Wirt: Synthetic
BP, WB
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- Target Alle Growth Hormone Receptor (GHR) Produkte
- Growth Hormone Receptor (GHR)
- Protein Region
- N-Term
- Spezies
- Human
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Quelle
- Synthetic
- Applikation
- Blocking Peptide (BP), Western Blotting (WB)
- Produktmerkmale
- This is a synthetic peptide designed for use in combination with anti-GHR antibody (Catalog #: ARP44230_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.
- Aufreinigung
- Purified
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-
- Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Konzentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handhabung
- Avoid repeated freeze-thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- Growth Hormone Receptor (GHR)
- Synonyme
- GHBP Peptide, AA986417 Peptide, GHR/BP Peptide, GHR Peptide, ghr Peptide, ghr.a Peptide, zgc:162141 Peptide, growth hormone receptor Peptide, growth hormone receptor L homeolog Peptide, growth hormone receptor a Peptide, GHR Peptide, Ghr Peptide, ghr.L Peptide, ghr Peptide, ghra Peptide
- Hintergrund
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GHR is a protein that is a transmembrane receptor for growth hormone. Binding of growth hormone to the receptor leads to receptor dimerization and the activation of an intra- and intercellular signal transduction pathway leading to growth. A common alternate allele of this gene, called GHRd3, lacks exon three and has been well-characterized. Mutations in this gene have been associated with Laron syndrome, also known as the growth hormone insensitivity syndrome (GHIS), a disorder characterized by short stature.This gene encodes a protein that is a transmembrane receptor for growth hormone. Binding of growth hormone to the receptor leads to receptor dimerization and the activation of an intra- and intercellular signal transduction pathway leading to growth. A common alternate allele of this gene, called GHRd3, lacks exon three and has been well-characterized. Mutations in this gene have been associated with Laron syndrome, also known as the growth hormone insensitivity syndrome (GHIS), a disorder characterized by short stature. Other splice variants, including one encoding a soluble form of the protein (GHRtr), have been observed but have not been thoroughly characterized. 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: GHBP
Protein Interaction Partner: AP2A1,CISH,GH2,GHR,GRB10,GRB2,IRS1,JAK1,JAK2,NCOA6,PIK3R1,PRLR,PTPN11,PTPN2,PTPN6,SGTA,SHC1,SOCS1,SOCS2,SOCS3,STAT3,STAT5A,STAT5B,TYK2,BTRC,CISH,GH1,GRB10,GRB2,JAK1,JAK2,PIK3R1,PLCG1,PTPN11,SGTA,SHC1,SOCS1,SOCS2,SOCS3,STAT3,STAT5B,TYK2
Protein Size: 638 - Molekulargewicht
- 70 kDa
- Gen-ID
- 2690
- NCBI Accession
- NM_000163, NP_000154
- UniProt
- P10912
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