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GABRG1 Blocking Peptide CBP5211
  • Western blot analysis of GABRG1 expression in LOVO (A), mouse brain (B) whole cell lysates.
  • Immunohistochemical analysis of GABRG1 staining in human brain formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugacompact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
Product NameGABRG1 Blocking Peptide
Cat No: CBP5211
Source: Synthetic
Reactivity: H, M, R
Applications: BL
*Application Key:
E- ELISA, WB - Western blot, IH - Immunohistochemistry, IF - Immunofluorescence, FC - Flow cytometry, IC - Immunocytochemistry, IP - Immunoprecipitation, ChIP - Chromatin Immunoprecipitation, EMSA - Electrophoretic Mobility Shift Assay, BL - Blocking, SE - Sandwich ELISA, CBE - Cell-based ELISA, RNAi - RNA interference
*Species Reactivity Key:
H - Human, M - Mouse, R - Rat, B - Bovine, C - Chicken, D - Dog, G - Goat, Mk - Monkey, P - Pig, Rb - Rabbit, S - Sheep, Z - Zebrafish
Size
Price
1 mg
$100
5 mg
$300
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Description: The peptide is used to block Anti-GABRG1 Antibody (#CPA5211) reactivity.
Form: Lyophilized powder
Gene Symbol: GABRG1
Alternative Names: Gamma-aminobutyric acid receptor subunit gamma-1; GABA(A) receptor subunit gamma-1
Entrez Gene (Human): 2565
Entrez Gene (Mouse) : 14405
Entrez Gene (Rat) : 140674
SwissProt (Human): Q8N1C3
SwissProt (Mouse) : Q9R0Y8
SwissProt (Rat) : P23574
Purity : >85%
Directions for Use : Blocking Peptide to the diluted primary antibody in a molar ratio of 10:1 (peptide to antibody) and incubate the mixture at 4°C for overnight or at room temperature for 2 hours.
Quality Control : The quality of the peptide was evaluated by reversed-phase HPLC and by mass spectrometry.
Storage/Stability : Shipped at 4°C. Store at -20°C for one year.
  • Western blot analysis of GABRG1 expression in LOVO (A), mouse brain (B) whole cell lysates.
  • Immunohistochemical analysis of GABRG1 staining in human brain formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugacompact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
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