Skip to main content

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-Thyroglobulin Antibody DL99683A



The add to cart button will appear once you select the values above

Specifications

50µl / 100µl

Background:

Mouse monoclonal antibody to Thyroglobulin

Alternative names:

Thyroglobulin; Tg

Clonality:

Monoclonal

Species reactivity:

H

Host:

Mouse

Immunogen:

KLH-conjugated synthetic peptide encompassing a sequence within human Thyroglobulin. The exact sequence is proprietary.

Purification method:

The antibody was purified by immunogen affinity chromatography.

Concentration:

1mg/mL

Buffer:

Mouse IgG1. Liquid in PBS containing 50% glycerol, 0.2% BSA and 0.01% sodium azide.

Applications:

IH

Recommended dilution:

IH (1/100 - 1/300)

Storage:

Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.

WB description:

N/A

IHC description:

Immunohistochemical analysis of Thyroglobulin staining in human papillary thyroid carcinoma 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:

Immunohistochemical analysis of Thyroglobulin staining in human thyroid follicular carcinoma 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.

IP description:

N/A

FC description:

N/A

ChIP description:

N/A

More info:

Email: info@sobekbio.com

Orders:

Email: orders@sobekbio.com