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DL Develop

DLDevelop

DLDevelop is a manufacturer of biological reagents for life science, headquartered in the scenic area beside the Taihu Lake. Founded in 1998, their company began business as an OEM service provider of ELISA kits across the world. In 2013, They launched their own brand, DLDevelop. DLDevelop specializes in manufacturing ELISA kits and their products have been distributed to the continents of Asia, Oceania, Africa, Europe and America. DLDevelop holds the tenet: “Quality first, Customer first”

www.dldevelop.com

Mouse anti-BCL2 Antibody DL95450A



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Specifications

50µl / 100µl

Background:

Mouse monoclonal antibody to BCL2

Alternative names:

Apoptosis regulator Bcl-2

Clonality:

Monoclonal

Species reactivity:

H, M, R

Host:

Mouse

Immunogen:

KLH-conjugated synthetic peptide encompassing a sequence of human BCL2. The exact sequence is proprietary.

Purification method:

Concentration:

1mg/mL

Buffer:

Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.

Applications:

WB, IHC, IF/IC

Recommended dilution:

WB (1/1000 - 1/2000), IH (1/200 - 1/500), IF/IC (1/100 - 1/200)

Storage:

Store at -20℃. Avoid repeated freeze / thaw cycles.

WB description:

Western blot analysis of BCL2 expression in Hela (A) whole cell lysates.

IHC description:

Immunohistochemical analysis of BCL2 staining in human tonsil 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.

IF/ICC description:

Immunofluorescent analysis of BCL2 staining in Hela 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 FITC-conjugated secondary antibody (green) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).

IP description:

N/A

FC description:

N/A

ChIP description:

N/A

More info:

Email: info@sobekbio.com

Orders:

Email: orders@sobekbio.com