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Anti-MNAT1 Rabbit Polyclonal Antibody #50499

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Immunohistochemical analysis of MNAT1 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 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 MNAT1 expression in HEK293T (A), Hela (B), mouse testis (C), mouse lung (D), rat lung (E) whole cell lysates.
  • 基因名:
    MNAT1
  • 货号:
    50499
  • 应用:
    WB, IHC
  • 物种反应性:
    H, M, R, B, P
规格:
20 μL,50 μL,100 μL
价格:
¥ 560.00,¥ 1,100.00,¥ 2,000.00
Information
Product Name Anti-MNAT1 Rabbit Polyclonal Antibody
Aliases CAP35; MAT1; RNF66; CDK-activating kinase assembly factor MAT1; CDK7/cyclin-H assembly factor; Cyclin-G1-interacting protein; Menage a trois; RING finger protein 66; RING finger protein MAT1; p35; p36
Background

Gene Name: MNAT1

NCBI Gene Entry: 4331

UniProt Entry: P51948

Application Information

Molecular Weight: Predicted, 35 kDa; observed, 36 kDa

Clonality: Rabbit polyclonal antibody

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

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

Immunogen A synthesized peptide derived from human MNAT1
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): 1:50-1:100
Note This product is for research use only.
Picture
  • Immunohistochemical analysis of MNAT1 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 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 MNAT1 expression in HEK293T (A), Hela (B), mouse testis (C), mouse lung (D), rat lung (E) whole cell lysates.
Citation(0)
Immunohistochemical analysis of MNAT1 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 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 MNAT1 expression in HEK293T (A), Hela (B), mouse testis (C), mouse lung (D), rat lung (E) whole cell lysates.
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