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Anti-KRT14 Rabbit Polyclonal Antibody #52608

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Immunofluorescent analysis of Cytokeratin 14 staining in
MCF7 cells. Formalin-fixed cells were permeabilized with 0.1%
Triton X-100 in TBS for 5-10 minutes and blocked with 3%
BSA-PBS for 30 minutes at room temperature. Cells were
probed with the primary antibody in 3% BSA-PBS and
incubated overnight at 4 °C in a humidified chamber. Cells
were washed with PBST and incubated with a DyLight
594-conjugated secondary antibody (red) in PBS at room
temperature in the dark.
Immunohistochemical analysis of Cytokeratin 14 staining in
human breast cancer 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 Cytokeratin 14 expression in MCF7
(A), mouse brain (B), rat brain (C) whole cell lysates.
  • 基因名:
    KRT14
  • 货号:
    52608
  • 应用:
    WB, IHC, IC
  • 物种反应性:
    H, M, R
规格:
20 μL,50 μL,100 μL
价格:
¥ 560.00,¥ 1,100.00,¥ 2,000.00
Information
Product Name Anti-KRT14 Rabbit Polyclonal Antibody
Aliases KRT14; Keratin 14; Keratin, Type I Cytoskeletal 14; Keratin 14, Type I; EBS3; EBS4; K14; Keratin 14 (Epidermolysis Bullosa Simplex, Dowling-Meara, Koebner); Epidermolysis Bullosa Simplex, Dowling-Meara, Koebner; Cytokeratin 14; Cytokeratin-14; Keratin-14; EBS1A; EBS1B; EBS1C; EBS1D; CK-14; CK14; EBS1; NFJ
Background

Gene Name: KRT14

NCBI Gene Entry: 3861

UniProt Entry: P02533

Application Information

Molecular Weight: Predicted, 51 kDa, observed, 52 kDa

Clonality: Rabbit polyclonal antibody

Species Reactivity: Human, mouse, rat

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

Immunogen A synthesized peptide derived from human KRT14
Isotype Rabbit IgG
Storage Buffer Supplied in PBS containing 50% glycerol, 0.5% BSA and 0.04% 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
Immunocytochemistry (IC): 1:100-1:500
Note This product is for research use only.
Picture
  • Immunofluorescent analysis of Cytokeratin 14 staining in
    MCF7 cells. Formalin-fixed cells were permeabilized with 0.1%
    Triton X-100 in TBS for 5-10 minutes and blocked with 3%
    BSA-PBS for 30 minutes at room temperature. Cells were
    probed with the primary antibody in 3% BSA-PBS and
    incubated overnight at 4 °C in a humidified chamber. Cells
    were washed with PBST and incubated with a DyLight
    594-conjugated secondary antibody (red) in PBS at room
    temperature in the dark.
  • Immunohistochemical analysis of Cytokeratin 14 staining in
    human breast cancer 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 Cytokeratin 14 expression in MCF7
    (A), mouse brain (B), rat brain (C) whole cell lysates.
Citation(0)
Immunofluorescent analysis of Cytokeratin 14 staining in
MCF7 cells. Formalin-fixed cells were permeabilized with 0.1%
Triton X-100 in TBS for 5-10 minutes and blocked with 3%
BSA-PBS for 30 minutes at room temperature. Cells were
probed with the primary antibody in 3% BSA-PBS and
incubated overnight at 4 °C in a humidified chamber. Cells
were washed with PBST and incubated with a DyLight
594-conjugated secondary antibody (red) in PBS at room
temperature in the dark.
Immunohistochemical analysis of Cytokeratin 14 staining in
human breast cancer 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 Cytokeratin 14 expression in MCF7
(A), mouse brain (B), rat brain (C) whole cell lysates.
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