Mouse Retinoic acid receptor responder protein 2(RARRES2) ELISA kit

Code CSB-EL019342MO
Size 96T,5×96T,10×96T
Price Request a Quote or Start an on-line Chat
Trial Size 24T ELISA Kit Trial Size (Only USD$150/ kit)
* The sample kit cost can be deducted from your subsequent orders of 96T full size kits of the same analyte at 1/5 per kit, until depleted in 6 months. Apply now

Product Details

Target Name
retinoic acid receptor responder (tazarotene induced) 2
Alternative Names
Rarres2 ELISA Kit; Retinoic acid receptor responder protein 2 ELISA Kit; Chemerin ELISA Kit
Abbreviation
RARRES2
Uniprot No.
Species
Mus musculus (Mouse)
Sample Types
serum, plasma, tissue homogenates
Detection Range
0.625 ng/mL-40 ng/mL
Sensitivity
0.411 ng/mL
Assay Time
1-5h
Sample Volume
50-100ul
Detection Wavelength
450 nm
Research Area
Cardiovascular
Assay Principle
quantitative
Measurement
Sandwich
Troubleshooting
and FAQs
Storage
Store at 2-8°C. Please refer to protocol.
Lead Time
3-5 working days after you place the order, and it takes another 3-5 days for delivery via DHL or FedEx
Description

This Mouse RARRES2 ELISA Kit was designed for the quantitative measurement of Mouse RARRES2 protein in serum, plasma, tissue homogenates. It is a Sandwich ELISA kit, its detection range is 0.625 ng/mL-40 ng/mL and the sensitivity is 0.411 ng/mL.

Customer Reviews and Q&A

 Customer Reviews

There are currently no reviews for this product.

Submit a Review here

Target Background

Function
(From Uniprot)
Adipocyte-secreted protein (adipokine) that regulates adipogenesis, metabolism and inflammation through activation of the chemokine-like receptor 1 (CMKLR1). Acts also as a ligand for CMKLR2. Can also bind to C-C chemokine receptor-like 2 (CCRL2), but with a lower affinity than it does to CMKLR1 or CMKLR2. Positively regulates adipocyte differentiation, modulates the expression of adipocyte genes involved in lipid and glucose metabolism and might play a role in angiogenesis, a process essential for the expansion of white adipose tissue. Also acts as a proinflammatory adipokine, causing an increase in secretion of proinflammatory and prodiabetic adipokines, which further impair adipose tissue metabolic function and have negative systemic effects including impaired insulin sensitivity, altered glucose and lipid metabolism, and a decrease in vascular function in other tissues. Can have both pro- and anti-inflammatory properties depending on the modality of enzymatic cleavage by different classes of proteases. Acts as a chemotactic factor for leukocyte populations expressing CMKLR1, particularly immature plasmacytoid dendritic cells, but also immature myeloid DCs, macrophages and natural killer cells. Exerts an anti-inflammatory role by preventing TNF/TNFA-induced VCAM1 expression and monocytes adhesion in vascular endothelial cells. The effect is mediated via inhibiting activation of NF-kappa-B and CRK/p38 through stimulation of AKT1/NOS3 signaling and nitric oxide production. Exhibits an antimicrobial function in the skin.
Gene References into Functions
  1. Systemic and hepatic chemerin, and chemerin receptor activation were not changed in hepatocellular carcinoma. Chemerin protein was induced in liver in NASH, but was unchanged in HCC tissues. Hepatic and serum chemerin and ex vivo analyzed chemerin receptor activation do not differ in murine NASH-associated HCC when compared to NASH. PMID: 29715085
  2. endogenously secreted chemerin plays an autocrine/paracrine role in white adipose tissue, identifying chemerin as a therapeutic target to modulate adipose remodelling. PMID: 27461525
  3. elevated levels of chemerin were found in colons of mice with experimental colitis, and a neutralizing anti-chemerin antibody improved intestinal inflammation PMID: 24727542
  4. Data suggest a potential role for chemerin and CMKLR1 in the regulation of inflammatory responses in the tumor microenvironment. PMID: 21752353
  5. Suggest reduction of chemerin could contribute to the antiobesity/antidiabetic properties described for alpha-lipoic acid. PMID: 26721419
  6. Study indicates that Chemerin plays a role in the negative cross-talk between skeletal muscle and adipose tissue. Specifically, Chemerin promotes the adipogenic differentiation potential and alters the myoblast cell fate from myogenesis to adipogenesis. PMID: 26164089
  7. Data indicate that chemerin may play an important role in regulating mitochondrial remodelling and function in skeletal muscle. PMID: 25754411
  8. The chemerin15 (C15) precursor, chemerin, and its receptor, ChemR23, are both upregulated after skin damage and the receptor is expressed by macrophages, neutrophils, and keratinocytes. C15 delivery dampens immediate inflammatory events. PMID: 24881877
  9. findings reveal previously uncharacterized regulators of chemerin expression in skin and identify a physiologic role for chemerin in skin barrier defense against microbial pathogens. PMID: 25659101
  10. A novel autocrine/paracrine role for chemerin in regulating osteoclast differentiation of hematopoietic stem cells PMID: 23766088
  11. this study reports that retinoic acid-activated endothelial cells can promote myeloid and plasmacytoid dendritic cell transmigration across endothelial cell monolayers through the endogenous production of chemerin PMID: 24470498
  12. Data suggest that chemerin/ChemR23 (chemokine-like receptor 1) signaling is not essential for adipocyte differentiation, but it appears to play a role in control of body weight and energy metabolism as overweight/obesity progresses. PMID: 24084834
  13. Studies using isolated islets and perfused pancreas revealed impaired glucose-dependent insulin secretion (GSIS) in chemerin-deficient mice. Conversely, chemerin transgenic mice revealed enhanced GSIS and improved glucose tolerance. PMID: 22355640
  14. Following TNFalpha treatment, increased elastase and tryptase modify the balance between activation and deactivation, elevating active chemerin concentration in adipocyte media and subsequent CMKLR1 activation. PMID: 23227233
  15. results of this study indicate that chemerin plays a role in the negative cross-talk between skeletal muscle and adipose tissue to regulate myogenesis PMID: 22906999
  16. Downstream targets of Chemerin/ChemR23 signaling are phosphorylated in vitro and are expressed in mouse tooth development, suggesting roles for Chemerin/ChemR23-mediated epithelial-mesenchymal cell signaling during tooth morphogenesis. PMID: 23053848
  17. These results rule out the direct anti-inflammatory effect of chemerin on macrophages ex vivo, described previously in the literature, despite the expression of a functional ChemR23 receptor in these cells. PMID: 22768214
  18. Chemerin increases in airways during viral infection; Chemerin appears to have anti-inflammatory properties, by acting on ChemR23 expressed by non-leukocytic cells dampening the inflammatory response promoted by the viral infection; the chemerin/ChemR23 system plays important roles in the physiopathology of viral pneumonia PMID: 22072972
  19. a fundamental role for chemerin/CMKLR1 signaling in clonal expansion during adipocyte differentiation as well as a role for PPARgamma in regulating chemerin expression. PMID: 21572083
  20. The current data show that adipocyte hypertrophy and chronic inflammation are equally important in inducing chemerin synthesis. PMID: 21084441
  21. Macrophage chemoattractant protein chemerin, which is generated at sites of inflammation, rapidly stimulates adhesion of peritoneal macrophages to fibronectin and VCAM-1 by promoting clustering of integrins VLA-5 and VLA-4, respectively. PMID: 20720202
  22. data support a novel role for chemerin/CMKLR1 signaling in regulating adipogenesis and osteoblastogenesis of bone marrow-derived precursor cells PMID: 19929432
  23. Results identified TNFalpha as a positive regulator of adipocyte-derived chemerin. PMID: 20363880
  24. Ablation of the chemerin gene RARRES-2 may result in mice with a more overt phenotype than that of ChemR23-deficient mice through removal of chemerin-derived ligands for ChemR23. PMID: 20363975
  25. Data provide evidence that serum chemerin levels are elevated in obesity and diabetes. PMID: 20228173
  26. chemerin is a novel adipose-derived signaling molecule that regulates adipogenesis and adipocyte metabolism PMID: 17635925
  27. Thus, the adipokine chemerin likely regulates adipocyte function by autocrine/paracrine mechanisms. PMID: 17767914
  28. These data establish that chemerin is a novel adipokine that regulates adipocyte function. PMID: 18242188
  29. Interleukin-1beta induces the novel adipokine chemerin in adipocytes in vitro. PMID: 19233230
  30. Rarres2 is highly expressed in adipose tissue and during adipocyte differentiation. PMID: 17640997

Show More

Hide All

Subcellular Location
Secreted.
Tissue Specificity
Expressed in the differentiated adipocytes (at protein level). Abundantly expressed in the liver, adipose tissue including visceral, epididymal, and brown adipose tissue.
Database Links
icon of phone
Call us
301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)
icon of address
Address
7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
icon of social media
Join us with

Subscribe newsletter

Leave a message

* To protect against spam, please pass the CAPTCHA test below.
CAPTCHA verification
© 2007-2024 CUSABIO TECHNOLOGY LLC All rights reserved. 鄂ICP备15011166号-1