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Anti-METAP1 Antibody CQA9316
  • Western blot analysis of METAP1 expression in A549 (A) whole cell lysates.
  • Immunohistochemical analysis of METAP1 staining in human small intestine 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 conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
Product NameAnti-METAP1 Antibody
Cat No: CQA9316
Source: Mouse
Reactivity: H
Applications: WB
*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
200 μl
$350
100 μl
$220
50 μl
$150
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Description: Mouse monoclonal antibody to METAP1
Immunogen: Recombinant fusion protein of human METAP1. The exact sequence is proprietary.
Purification: This antibody is purified through a protein G column.
Clonality: Monoclonal
Form: Mouse IgG1 kappa. Liquid in PBS, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Dilution: WB (1/500 - 1/1000), IH (1/100 - 1/500)
Gene Symbol: METAP1
Alternative Names: KIAA0094; Methionine aminopeptidase 1; MAP 1; MetAP 1; Peptidase M 1
Entrez Gene (Human): 23173
SwissProt (Human): P53582
Storage/Stability : Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
  • Western blot analysis of METAP1 expression in A549 (A) whole cell lysates.
  • Immunohistochemical analysis of METAP1 staining in human small intestine 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 conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
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