anti-Desmoglein 2 mouse monoclonal, G96, supernatant

Cat. No: 651118

Available, delivery time 1-7 days

$269.00*

Key Features
  • Mouse monoclonal
  • Suitable for ELISA, IHC and WB
  • Reacts with human
  • Isotype: IgG1
Product description
Quantity 5 ml
Antibody Type Monoclonal
Host Mouse
Isotype IgG1
Conjugate Unconjugated
Application ELISA, IHC, WB
Purification Hybridoma cell culture supernatant
Reactivity Human
No reactivity Mouse, Rat
Storage Short term at 2-8°C; long term storage in aliquots at -20°C; avoid freeze/thaw cycles
Intended use Research use only
Clone G96
Immunogen Recombinant peptide (220aa of 2nd and 3rd extracellular repeat domain)
Formulation Contains 0.09% sodium azide
UniprotID Q14126 (Human)
Synonym Desmoglein-2, Cadherin family member 5, HDGC, DSG2, CDHF5
Applications
Tested applications Tested dilutions
Immunohistochemistry (IHC) - frozen Ready-to-use (for better resolution preincubation (directliy after fixation) with 0.05-0.2% Triton X-100, for 5-10 min, depending on tissue type, is recommended)
Immunohistochemistry (IHC) - paraffin Ready-to-use (microwave treatment recommended)
ELISA Assay dependent
Western Blot (WB) Assay dependent
Background

Antibody recognizes desmoglein 2 present in all epithelia and in tumors derived therefrom as well as in heart muscle and dendritic reticulum cells of lymphatic follicles. In basal epithelial cells desmoglein 2 expression is generally very low.

Polypeptide reacting: Desmoglein 2 (1069aa; calculated mol. wt. 116,760).

Recommended as positive control: CaCo-2, HaCaT.

Reactivities on Cultured cell lines: Many, including CaCo-2, HaCaT, MCF-7.

References/Publications (3)
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FAQs
The concentration of unpurified supernatant, ascites, unpurified guinea pig serum and unpurified rabbit serum is not determined.
The concentration of purified antibodies is mentioned on the datasheet.
For prediluted antibodies the concentration may vary from lot to lot. The concentration of these antibodies is not mentioned on the datasheet and can be requested at support@progen.com.

Most of our purified mouse antibodies contain 0.5% BSA as stabilizer. If BSA was added to the antibody solution, it is stated in the datasheet.
The supernatant format contains FCS proteins from cell culture medium supplemented with FCS.
The serum antibodies contain other proteins present in serum.

PROGEN offers different formats for mouse monoclonal antibodies.  Different antibodies may not be offered in each format, the following are all possible formats:
  1. Supernatant and supernatant concentrate: This format contains hybridoma cell culture supernatant. The antibody is not purified and the antibody concentration is not determined. The antibody concentration may vary from lot to lot. Therefore we recommend to titrate the optimal concentration for the application used for each new lot.
  2. Lyophilized, purified: This format contains purified antibody in lyophilized form. The reconstitution of this antibody is described in the datasheet. The buffer composition after reconstitution is also mentioned on the datasheet. 
  3. Liquid, purified: This format contains purified antibody in liquid format. The concentration is mentioned on the datasheet. 
  4. Prediluted, purified: This format contains purified antibody in liquid format. Most antibodies in this format are diluted to be ready-to-use for IHC with standard tissue. But some antibodies of this format need further dilution for IHC. This is mentioned on the datasheet.

Lyophilized antibodies can be stored at 2-8°C until expiration.
Most of our liquid antibodies and reconstituted lyophilized antibodies may be stored for short term storage (up to 3 month) at 2-8°C. For long term storage we recommend to store the antibody at -20°C in aliquots. Please avoid freeze and thaw cycles.
Most of our conjugated antibodies should be stored at 2-8°C.
The individual storage conditions are mentioned on the datasheet.

The expiration date of our antibodies is indicated on the product label.
We offer bulk amounts starting from 1 mg for many of our mouse monoclonal or recombinant antibodies. Please contact us for further information or use the “bulk button” on the product page?
Most of our antibodies contain 0.09% sodium azide as preservative. If a preservative is added, it is mentioned in the datasheet.
The optimal antibody dilution for your specific protocol and application needs to be titrated in your lab with your equipment and sample. The optimal dilution may vary between protocols and samples. A good dilution for starting the titration is the dilution mentioned in the datasheet. If the sample needs a specific treatment (eg. Antigen retrieval for IHC on FFPE sections) this should also be mentioned on the antibody datasheet. 
PROGEN antibodies are shipped at ambient temperature. The antibodies are stable at ambient temperature for the shipment period. Please store the antibodies as indicated in the datasheet upon arrival.
  • Homogenization of tissue in PBS (supplemented with protease inhibitors).
  • Centrifugation at 10E4 x g.
  • Optional: treat pellet with DNase.
  • Resuspend pellet in detergent buffer (e.g. 1% Triton X-100), stir for 1 h at 2-8°C.
  • Centrifugation at 10E4 x g.
  • Resuspend pellet in high salt buffer (with 1.5 M KCl), stir for 1 h at 2-8°C.
  • Centrifugation at 10E4 x g.
  • Resuspend pellet in low salt buffer (e.g. 50 mM NaCl), stir for 30 min at 2-8°C.
  • Centrifugation at 10E4 x g: pellet contains raw cytoskeletal fraction.

  • Transfer from a low concentration acrylamide gel (e.g. 8%).
  • Reduce the methanol concentration of the transfer buffer (limit is 50% of the routine concentration 20% methanol).
  • Use the wet transfer method and transfer at least 4 h (or better overnight) at 100-200 mA.
  • In order to prevent the accumulation of gas bubbles, stir the transfer buffer continuously during the transfer (e.g. with a magnetic stirrer).
  • If possible use a cytoskeletal preparation of your material to be analyzed (in the case of cultured cells additionally DNase treatment) rather than whole cell lysate.
  • As a general rule we would like to recommend loading that much protein into one gel lane that the intermediate filament polypeptides (in the 40-60 kD range) can be readily detected in a control gel stained with Coomassie blue.

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