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Anti-ATG16L1 Antibody CQA9430
  • Western blot analysis of ATG16L1 expression in ATG16L1 recombinant protein (A) whole cell lysates.
  • Immunohistochemical analysis of ATG16L1 staining in human lung carcinoma 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-ATG16L1 Antibody
Cat No: CQA9430
Source: Mouse
Reactivity: H
Applications: WB, IH
*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 ATG16L1
Immunogen: Recombinant fusion protein of human ATG16L1. 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 (1/1000 - 1/2000), IH (1/50 - 1/200)
Gene Symbol: ATG16L1
Alternative Names: APG16L; Autophagy-related protein 16-1; APG16-like 1
Entrez Gene (Human): 55054
SwissProt (Human): Q676U5
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 ATG16L1 expression in ATG16L1 recombinant protein (A) whole cell lysates.
  • Immunohistochemical analysis of ATG16L1 staining in human lung carcinoma 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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