Goldenhar Syndrome Antikörper (C-Term)
GHS
Reaktivität: Human, Maus
IHC (p), WB
Wirt: Kaninchen
Polyclonal
unconjugated
-
- Target
- Goldenhar Syndrome (GHS)
- Bindungsspezifität
- AA 326-357, C-Term
- Reaktivität
- Human, Maus
- Wirt
- Kaninchen
- Klonalität
- Polyklonal
- Applikation
- Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
- Aufreinigung
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogen
- This GHSR antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 326-357 amino acids from the C-terminal region of human GHSR.
- Isotyp
- Ig Fraction
-
- Applikationshinweise
-
For IHC-P starting dilution is: 1:50~100
For WB starting dilution is: 1:1000 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Format
- Liquid
- Konzentration
- 0.4 mg/mL
- Buffer
- Supplied in PBS with 0.09 % (W/V) sodium azide.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- 4 °C,-20 °C
- Informationen zur Lagerung
- Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
-
- Target
- Goldenhar Syndrome (GHS)
- Andere Bezeichnung
- GHS
- Synonyme
- Goldenhar syndrome antikoerper, GHS antikoerper
- Hintergrund
- This gene encodes a member of the G-protein coupled receptor family. The encoded protein may play a role in energy homeostasis and regulation of body weight. Two identified transcript variants are expressed in several tissues and are evolutionary conserved in fish and swine. One transcript, 1a, excises an intron and encodes the functional protein, this protein is the receptor for the Ghrelin ligand and defines a neuroendocrine pathway for growth hormone release. The second transcript (1b) retains the intron and does not function as a receptor for Ghrelin, however, it may function to attenuate activity of isoform 1a. Mutations in this gene are associated with autosomal idiopathic short stature.
- Molekulargewicht
- 41 kDa
- Gen-ID
- 2693
- UniProt
- Q92847
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