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Merck

DPP4-M

DPP IV Inhibitor

Synonyma:

DPP IV Inhibitor, Dipeptidyl peptidase 4 Inhibitor, Gliptins

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Vybrat velikost

1 ML

2 210,00 Kč

10 ML

14 200,00 Kč

2 210,00 Kč


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O této položce

UNSPSC Code:
41116012
NACRES:
NC.07
eCl@ss:
32160405

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form

solution

NCBI accession no.

UniProt accession no.

Quality Level

Gene Information

human ... DPP4(1803)

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D3822416200317642
Gene Information

human ... DPP4(1803)

Gene Information

-

Gene Information

-

Gene Information

-

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

form

solution

form

solid

form

amorphous solid

form

solid

NCBI accession no.

NM_001935.3

NCBI accession no.

-

NCBI accession no.

-

NCBI accession no.

-

UniProt accession no.

P27487

UniProt accession no.

-

UniProt accession no.

-

UniProt accession no.

-

Application

Research Category
All

Biochem/physiol Actions

Dipeptidyl peptidase IV (DPP IV) controls insulin-stimulating hormones, glucagon-like peptide (GLP-1), and glucose-dependent insulinotropic polypeptide (GIP). It′s a promising therapeutic target for type 2 diabetes (T2DM).[1] In addition to its catalytic action, DPP-4 also serves as a binding protein and a ligand of extracellular factors.[2] DPP-4 inhibition causes GLP-1 and GIP to have a prolonged activity, hence DPP-4 inhibitors help maintain glucose homeostasis. DPP IV inhibitors can improve glycemic control for a longer period when compared to early oral hypoglycemics.[3]

General description

Dipeptidyl peptidase IV (DPP IV), a dimeric type II integral membrane glycoprotein, is a member of the family of prolyl-specific proteases. It is abundantly expressed in the epithelial and nonepithelial tissues. It is highly expressed in the kidney and the colon.[4]

Preparation Note

Upon arrival, store at 4°C. For long-term of more than 2 weeks, store at –20°C.

Osvědčení o analýze (COA)

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Navštívit knihovnu dokumentů

Rajesh Gupta et al.
Current drug targets, 10(1), 71-87 (2009-01-20)
Dipeptidyl peptidase IV (DPP IV) is a key regulator of insulin-stimulating hormones, glucagon-like peptide (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), thus it is a promising target for the treatment of Type 2 Diabetes mellitus (T2DM). Inhibition of plasma DPP IV
Sebastiano Bruno Solerte et al.
Acta diabetologica, 57(7), 779-783 (2020-06-09)
SARS-CoV-2 causes severe respiratory syndrome (COVID-19) with high mortality due to a direct cytotoxic viral effect and a severe systemic inflammation. We are herein discussing a possible novel therapeutic tool for COVID-19. Virus binds to the cell surface receptor ACE2;
Sourav De et al.
Mini reviews in medicinal chemistry, 19(2), 88-97 (2018-04-26)
Diabetes mellitus is an emerging predator and affecting around 422 million adults worldwide. Higher levels of circulating insulin and increased pressure on the pancreas to produce insulin have been inferred as possible etiology for diabetes leading to a higher risk
Lucienne Juillerat-Jeanneret
Journal of medicinal chemistry, 57(6), 2197-2212 (2013-10-09)
The proline-specific dipeptidyl aminopeptidase IV (DPP IV, DPP-4, CD26), widely expressed in mammalians, releases X-Pro/Ala dipeptides from the N-terminus of peptides. DPP IV is responsible of the degradation of the incretin peptide hormones regulating blood glucose levels. Several families of

Questions

1–2 of 2 Questions  
  1. Would our lab be able to store this product at -80 degrees celsius without compromising its composition? 

    1 answer
    1. It is recommended to store this product at -20°C. The long term stability of this product at -80°C has not been determined. However, there are no issues anticipated by storing this material at ultra-low temperatures.

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  2. What is the concentration of this product and what is the working concentration suggested? Thanks!

    1 answer
    1. This product as provided at a concentration of 4 mM. The working concentration recommendations are 10 μl/mL of whole blood or 20 μl/mL of buffer, plasma, serum, or tissue culture medium. These are general usage recommendations, the optimal concentration is application- and/or system-dependent. The final working concentration should be empirically determined by the end user.

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