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Anti-ANKRD1 Rabbit Polyclonal Antibody #51184

一键复制产品信息
Immunohistochemical analysis of ANKRD1 staining in human lymph node 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.
Western blotting analysis of ANKRD1 expression in mouse muscle (A), rat muscle (B) whole cell lysates.
  • 基因名:
    ANKRD1
  • 货号:
    51184
  • 应用:
    WB, IHC
  • 物种反应性:
    H, M, R, B, C, P, Rb
规格:
20 μL,50 μL,100 μL
价格:
¥ 560.00,¥ 1,100.00,¥ 2,000.00
Information
Product Name Anti-ANKRD1 Rabbit Polyclonal Antibody
Aliases C193; CARP; HA1A2; Ankyrin repeat domain-containing protein 1; Cardiac ankyrin repeat protein; Cytokine-inducible gene C-193 protein; Cytokine-inducible nuclear protein
Background

Gene Name: ANKRD1

NCBI Gene Entry: 27063

UniProt Entry: Q15327

Application Information

Molecular Weight: Predicted, 36 kDa; observed, 43 kDa

Clonality: Rabbit polyclonal antibody

Species Reactivity: Human, mouse, rat, bovine, chicken, pig, rabbit

Applications Tested: Western blotting (WB), immunohistochemistry (IHC)

Immunogen A synthesized peptide derived from human ANKRD1
Isotype Rabbit IgG
Storage Buffer Supplied in PBS (pH 7.3) containing 30% glycerol, and 0.01% sodium azide.
Storage Store at -20 °C for one year.
Recommended Dilutions Western Blotting (WB): 1:500-1:1,000
Immunohistochemistry (IHC): 1:100-1:200
Note This product is for research use only.
Picture
  • Immunohistochemical analysis of ANKRD1 staining in human lymph node 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.
  • Western blotting analysis of ANKRD1 expression in mouse muscle (A), rat muscle (B) whole cell lysates.
Citation(0)
Immunohistochemical analysis of ANKRD1 staining in human lymph node 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.
Western blotting analysis of ANKRD1 expression in mouse muscle (A), rat muscle (B) whole cell lysates.
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