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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

Rabbit anti-TMEM16J Antibody DL94316A



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Specifications

50µl / 100µl

Background:

Rabbit polyclonal antibody to TMEM16J

Alternative names:

PIG5; TMEM16J; TP53I5; Anoctamin-9; Transmembrane protein 16J; Tumor protein p53-inducible protein 5; p53-induced gene 5 protein

Clonality:

Polyclonal

Species reactivity:

H, M

Host:

Rabbit

Immunogen:

KLH-conjugated synthetic peptide encompassing a sequence within the center region of human TMEM16J. The exact sequence is proprietary.

Purification method:

The antibody was purified by immunogen affinity chromatography.

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 (1/500 - 1/2000), IH (1/50 - 1/200), IF/IC (1/50 - 1/100)

Storage:

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

WB description:

Western blot analysis of TMEM16J expression in RAW264.7 (A) whole cell lysates.

IHC description:

Immunohistochemical analysis of TMEM16J 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.

IF/ICC description:

Immunofluorescent analysis of TMEM16J staining in HepG2 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. 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