Przejdź do zawartości
Merck
Wszystkie zdjęcia(3)

Key Documents

MABS1166

Sigma-Aldrich

Anti-AdipoR2 Antibody, clone 4D3.2

clone 4D3.2, from mouse

Synonim(y):

Adiponectin receptor protein 2, AdipoR2, Progestin and adipoQ receptor family member II

Zaloguj sięWyświetlanie cen organizacyjnych i kontraktowych


About This Item

Kod UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.41

pochodzenie biologiczne

mouse

Poziom jakości

forma przeciwciała

purified immunoglobulin

rodzaj przeciwciała

primary antibodies

klon

4D3.2, monoclonal

reaktywność gatunkowa

human, rat

metody

immunohistochemistry: suitable (paraffin)
western blot: suitable

izotyp

IgG1κ

numer dostępu NCBI

numer dostępu UniProt

Warunki transportu

wet ice

docelowa modyfikacja potranslacyjna

unmodified

informacje o genach

human ... ADIPOR2(79602)

Opis ogólny

Adiponectin receptor protein 2 (UniProt Q86V24; also known as Progestin and adipoQ receptor family member II) is encoded by the ADIPOR2 (also known as PAQR2) gene (Gene ID 79602) in human. Adiponectin receptor protein 1 & 2 (AdipoR1 & AdipoR2) are receptors for adiponectin, a well knonwn anti-inflammatory adipokine highly abundant in serum. Both AdipoR1 and AdipoR2 are reported to be ubiquitously expressed with the highest expression in skeletal muscle and liver, respectively. Circulating adiponectin levels are reduced in obesity and type II diabetes, whereas weight loss elevates serum adiponectin. Adiponectin deficiency in mice is reported to exacerbate metabolic dysfunction by diet-induced obesity in some studies, while adiponectin overexpression alleviates metabolic dysfunction independent of weight loss in both genetic and diet-induced animal models of obesity. Adipor1-knockout (KO) results in increased adiposity and decreased glucose clearance in mice, whereas Adipor2-KO mice are lean and displayed improved glucose clearance. In addition to its metabolic role, adiponectin deficiency is associated with various clinical cardiovascular disorders including myocardial infarction, peripheral artery disease, and endothelial dysfunction. In a study of murine hind limb ischemia model, blood flow recovery after chronic hind limb ischemic surgery is similar among wild-type and AdipoR1-KO mice, while revascularization in AdipoR2-KO mice is severely attenuated. Human AdipoR2 is a 7-transmembrane (a.a. 148-168, 182-202, 214-234, 246-266, 274-294, 310-330, 349-369) protein with the opposite topology of G protein-coupled receptors (GPCRs), having its N-terminal end at the cytoplasmic side (a.a. 1-147) and C-terminal end at the extracellular side (a.a. 370-386). Unlike GPCRs also, adipoR1 & AdipoR2 transmembrane helices are not kinked or tilted relative to the plane of the membrane.

Specyficzność

Clone 4D3.2 targets an epitope within the N-terminal cytoplasmic domain.

Immunogen

Epitope: N-terminal cytoplasmic domain.
GST-tagged recombinant human AdipoR2 N-terminal fragment.

Zastosowanie

Immunohistochemistry Analysis: A 1:250 dilution from a representative lot detected AdipoR2 in human prostate cancer, as well as normal rat heart and human cerebral cortex tissue sections.
Research Category
Signaling
Research Sub Category
Lipid Metabolism & Weight Regulation
This Anti-AdipoR2 Antibody, clone 4D3.2 is validated for use in Western Blotting, Immunohistochemistry (Paraffin) for the detection of AdipoR2.

Jakość

Evaluated by Western Blotting of GST-tagged human AdipoR2 N-terminal fragment.

Western Blotting Analysis: A 1:1000 dilution of this antibody detected 50 ng of GST-tagged recombinant human AdipoR2 N-terminal fragment.

Opis wartości docelowych

43.88 kDa calculated.

Postać fizyczna

Format: Purified
Protein G purified.
Purified mouse monoclonal IgG1κ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Przechowywanie i stabilność

Stable for 1 year at 2-8°C from date of receipt.

Inne uwagi

Concentration: Please refer to lot specific datasheet.

Oświadczenie o zrzeczeniu się odpowiedzialności

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
This page may contain text that has been machine translated.

Nie możesz znaleźć właściwego produktu?  

Wypróbuj nasz Narzędzie selektora produktów.

Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


Certyfikaty analizy (CoA)

Poszukaj Certyfikaty analizy (CoA), wpisując numer partii/serii produktów. Numery serii i partii można znaleźć na etykiecie produktu po słowach „seria” lub „partia”.

Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Kiyoharu J Miyagishima et al.
Communications biology, 4(1), 1360-1360 (2021-12-11)
Late-onset retinal degeneration (L-ORD) is an autosomal dominant disorder caused by a missense substitution in CTRP5. Distinctive clinical features include sub-retinal pigment epithelium (RPE) deposits, choroidal neovascularization, and RPE atrophy. In induced pluripotent stem cells-derived RPE from L-ORD patients (L-ORD-iRPE)

Nasz zespół naukowców ma doświadczenie we wszystkich obszarach badań, w tym w naukach przyrodniczych, materiałoznawstwie, syntezie chemicznej, chromatografii, analityce i wielu innych dziedzinach.

Skontaktuj się z zespołem ds. pomocy technicznej