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Cusabio

SKU:CSB-RA148565A0HU

MAPK7 Recombinant Monoclonal Antibody

MAPK7 Recombinant Monoclonal Antibody

Regular price $350.00 USD
Regular price Sale price $350.00 USD
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Size
Release Date 2025-10-28
Product Code CSB-RA148565A0HU
Short Name MAPK7 Recombinant Monoclonal Antibody
Antibody Type Recombinant Antibody
List Price $350/100ul, $210/50ul
Species Reactivity Human, Mouse, Rat
Tested Applications ELISA, WB, IHC, IF
Dilution WB:1:500-1:5000, IHC:1:50-1:200, IF:1:50-1:200
Purification Method Affinity chromatography
Buffer Formulation PBS, 150mM NaCl, 50% Glycerol, 0.05% BSA, 0.02% Sodium Azide, pH 7.4.
Antigen A synthesized peptide from human MAPK7 protein
Antigen Species Human
Uniprot ID Q13164
Target Name MAPK7
Clonality Monoclonal
Clone ID 19F12
Host Species Rabbit
Isotype IgG
Conjugation Non-conjugated
Form Liquid
Storage Condition Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze.
TDS URL https://www.cusabio.com/datasheet/12946094/
Size 100ul

Image 1

Western Blot
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Positive WB detected in:Hela whole cell lysate(30µg), MCF-7 whole cell lysate(30µg), Jurkat whole cell lysate(30µg), HEK293 whole cell lysate(30µg), COLO-205 whole cell lysate(30µg), SH-SY5Y whole cell lysate(30µg), Mouse brain tissue lysate(30µg), Rat brain tissue lysate(30µg)

All lanes: ERK5 antibody at 1:1000

Secondary

Goat polyclonal to rabbit IgG at 1/40000 dilution

Predicted band size: 88 kDa

Observed band size: 115 kDa

Exposure time:2min

Image 2

IHC image of CSB-RA148565A0HU diluted at 1:100 and staining in paraffin-embedded human stomach tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.

Image 3

IHC image of CSB-RA148565A0HU diluted at 1:100 and staining in paraffin-embedded human liver cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.

Image 4

Immunofluorescence staining of Hela cell with CSB-RA148565A0HU at 1:50 , counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).

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