Browse our Adiponectin (ADIPOQ) ELISA Kits

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Adiponectin, C1Q and Collagen Domain Containing ELISA Kits (ADIPOQ)
On are 0 Adiponectin, C1Q and Collagen Domain Containing (ADIPOQ) ELISA Kits from different suppliers available. A total of 0 Adiponectin products are currently listed.
30kDa, Acdc, Acrp30, adipo, ADIPOQ, ADIPQTL1, ADN, ADPN, APM-1, apM1, APN, GBP28, MGC84292
list all ELISA KIts Gene Name GeneID UniProt
Human ADIPOQ ADIPOQ 9370 Q15848
Mouse ADIPOQ ADIPOQ 11450 Q60994
Rat ADIPOQ ADIPOQ 246253  

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More ELISA Kits for Adiponectin Interaction Partners

Rhesus Monkey Adiponectin, C1Q and Collagen Domain Containing (ADIPOQ) interaction partners

  1. The effects of exogenous human kisspeptin-10 (KP10) were studied on three important adipokines, namely, adiponectin, leptin (show LEP ELISA Kits), and resistin (show RETN ELISA Kits) in a set of four chair-restraint habituated intact adult male rhesus monkeys.

Rabbit Adiponectin, C1Q and Collagen Domain Containing (ADIPOQ) interaction partners

  1. Adiponectin level partially reflects the severity of liver steatosis, but not the degree of liver inflammation.

Human Adiponectin, C1Q and Collagen Domain Containing (ADIPOQ) interaction partners

  1. ADIPOQ expression was lower in the knee synovium of obese patients compared to lean patients.

  2. Findings suggest that in spite of the nonsignificant association between adiponectin (ADIPOQ) T45G or G276T polymorphism and hypertension, the heterozygous mutation of G276T was observed to account for increased levels of circulating adiponectin and blood pressure, especially in hypertensive patients.

  3. Adipoq KO dams developed glucose intolerance and hyperlipidemia in late pregnancy. Increased fetal body weight was detected in Adipoq KO dams. Hepatic glucose and triglyceride production rates of Adipoq KO dams were significantly higher than those of WT dams. Robustly enhanced lipolysis was found in gonadal fat of Adipoq KO dams. Maternal adiponectin deficiency does not reduce insulin (show INS ELISA Kits) sensitivity.

  4. Adiponectin levels increased significantly in both groups of patients after surgery: in patients undergoing reduction mammaplasty and abdominoplasty, the mean increase was equal to 1.68 (P = 0.007) and 4.28 (P = 0.019), respectively. The effective correlation between the role of breast adipose tissue and appearance of disease is still to be determined.

  5. Centenarians had significant higher serum levels of leptin (show LEP ELISA Kits) compared with controls (p<0.001), whereas no significant differences were observed for adiponectin.

  6. Incidence rate of metabolic syndrome was the highest in subjects with low serum adiponectin levels and high visceral fat area.

  7. This study suggested that adiponectin plays a significant role in human sebaceous gland biology.

  8. ADIPOQ variants rs2241766 T/G, rs1501299 G/T had a population specific correlation with colorectal cancer, which may be mediated by insulin (show INS ELISA Kits) resistance ( Meta-Analysis)

  9. low adiponectin concentrations are associated with a higher prevalence of subclinical atherosclerosis, independent of traditional cardiovascular risk factors.

  10. Adiponectin circulating levels are inversely and independently associated with muscular fitness in Portuguese adolescents.

Mouse (Murine) Adiponectin, C1Q and Collagen Domain Containing (ADIPOQ) interaction partners

  1. Irisin (show FNDC5 ELISA Kits) improved endothelial function by modulating HO-1 (show HMOX1 ELISA Kits)/ adiponectin axis in perivascular adipose tissue (PVAT) in HFD-induced obese mice. These findings suggest that regulating PVAT function may be a potential mechanism by which irisin (show FNDC5 ELISA Kits) improves endothelial function in obesity.

  2. a unique key feature of the T-cad (show CDH13 ELISA Kits) prodomain is its involvement in binding of the T-cad (show CDH13 ELISA Kits) repeats 1 and 2 to adiponectin; adiponectin positively regulates T-cad (show CDH13 ELISA Kits) abundance

  3. adiponectin maintains intestinal homeostasis and protects against murine colitis through interactions with its receptor AdipoR1 (show ADIPOR1 ELISA Kits) and by modulating adaptive immunity and STAT3 (show STAT3 ELISA Kits) signaling

  4. The KIF5B (show KIF5B ELISA Kits) level was up-regulated during 3T3-L1 adipogenesis. This increase in cytosolic KIF5B (show KIF5B ELISA Kits) was synchronized with the induction of adiponectin. Endogenous KIF5B (show KIF5B ELISA Kits) and adiponectin were partially colocalized at the peri (show POSTN ELISA Kits)-nuclear and cytosolic regions.

  5. The elevation in circulating levels of adiponectin and Fgf15 led to normalized hepatic and serum levels of bile acids, limited hepatic accumulation of toxic bile, attenuated inflammation, and amelioration of liver injury in the ethanol-fed mNT knockout mice.

  6. Female adiponectin null mice displayed impaired fertility, reduced oocytes, disrupted estrous cycle, increased atretic follicles, and impaired late folliculogenesis. There was decrease in serum estradiol and FSH but an increase in LH and testosterone at proestrus. There was reduction of progesterone levels at diestrus, a significant decrease in LH receptor expression as well as in the number of GnRH immunoreactive neurons

  7. Tongqiaohuoxue decoction improved obesity-induced inflammation and insulin (show INS ELISA Kits) resistance by increasing adiponectin production.

  8. High salt is an important suppressor of cardioprotective APN (show ANPEP ELISA Kits) and AdipoR1 (show ADIPOR1 ELISA Kits) in cardiac myocytes.

  9. PPARdelta (show PPARD ELISA Kits) activation in perirenal fat by agonist or high sodium intake inhibited renal sodium-glucose cotransporter 2 (SGLT2 (show SLC5A2 ELISA Kits)) function, which is mediated by increased production of adipose adiponectin.

  10. Acute knockdown of Insr (show INSR ELISA Kits) or both Irs1 (show IRS1 ELISA Kits) and Irs2 (show IRS2 ELISA Kits) in adipocytes increased Adipoq mRNA expression but reduced adiponectin secretion.

Pig (Porcine) Adiponectin, C1Q and Collagen Domain Containing (ADIPOQ) interaction partners

  1. Results presented in this study indicate the modulatory effect of P4 on adiponectin system in the porcine uterus during early pregnancy, which may suggest the involvement of this adipokine in the early pregnancy establishment.

  2. The fluctuations in adiponectin and orexin concentrations in the plasma and uterine lining fluid (ULF) suggest that the hormones present in ULF are mostly of local origin and that these hormones participate in the processes that accompany early pregnancy.

  3. This study demonstrated the presence of adiponectin and its receptors in the uteri, conceptuses, and trophoblasts of pregnant pigs and that the local adiponectin system is dependent on the stage of pregnancy.

  4. It was concluded that the recombinant ADPN (show PNPLA3 ELISA Kits) could express in eukaryotic expression vector pPICZaA-ADPN (show PNPLA3 ELISA Kits) constructed in this study.

  5. study demonstrated that adiponectin and adiponectin receptors 1 and 2 messenger RNAs and proteins are present in the porcine hypothalamus and that their expression levels are determined by the pig's endocrine status related to the oestrous cycle

  6. This study demonstrated the presence of adiponectin, AdipoR1 (show ADIPOR1 ELISA Kits) and AdipoR2 (show ADIPOR2 ELISA Kits) genes and proteins in the porcine uterus and the effect of the stage of the oestrous cycle on the expression of the adiponectin system.

  7. inhibition of ADIPOQ gene changes the mRNA levels of the adipocyte differentiation transcription factors LPL (show LPL ELISA Kits), PPARgamma (show PPARG ELISA Kits) and AP2 (show TFAP2B ELISA Kits).

  8. Myocardial ADN (show CFD ELISA Kits) was reduced in dilated cardiomyopathy in an AMPK (show PRKAA1 ELISA Kits)-independent manner.

  9. Results indicated that PPARgamma (show PPARG ELISA Kits) is an essential regulatory factor for the transcriptional activity of ERp44 (show ERP44 ELISA Kits), which in turn controls the secretion of adiponectin.

  10. Adiponectin differentially regulates cytokines in porcine macrophages

Cow (Bovine) Adiponectin, C1Q and Collagen Domain Containing (ADIPOQ) interaction partners

  1. Low level expression of adiponectin mRNA was found in all areas of bovine mammary gland tissues examined. AdipoR1 (show ADIPOR1 ELISA Kits) and AdipoR2 (show ADIPOR2 ELISA Kits) mRNAs were also detected in mammary tissues and their expression was particularly prominent in the parenchyma and cistern.

  2. Data suggest that genetic variation in promoter region of ADIPOQ (SNPs g.81966235C>T, g.81966377T>C, and g.81966364D>I) contribute to adiposity/marbling in skeletal muscle/meat (and thus meat quality) of Hanwoo beef cattle of North Korea.

  3. These data suggest differential contribution of adipose tissue depots to circulating adiponectin.

  4. Association analysis indicated that variable duplication within the ADIPOQ gene is associated with body measurements.

  5. 14 polymorphisms of the ADIPOQ gene were observed in Chinese cattle; 2 polymorphisms PR_-135 A>G and PR_-68 G>C were located in the core promoter region of ADIPOQ; 3 haplotypes in the 2 polymorphic sites were detected which produce effects on ADIPOQ transcription and are associated with growth traits

  6. reduced plasma adiponectin belongs to the subset of hormonal adaptations in EL dairy cows facilitating mammary glucose uptake via promotion of insulin (show INS ELISA Kits) resistance

  7. The physiologic status of the ovary has significant effects on the natural expression patterns of adiponectin and its receptors in follicular and luteal cells of bovine ovary.

  8. The disulfide bonds help to maintain the mature octadecameric adiponectin structure and stabilize intermediates during the assembly.

  9. Gobular adiponectin increased NO production in aortic endothlium by increasing NO synthase (show NOS ELISA Kits) activity.

  10. results indicate decreasing adiponectin sensitivity in adipose tissue after calving which might be involved in the reduced insulin (show INS ELISA Kits) sensitivity of adipose tissue during lactation

Adiponectin (ADIPOQ) Antigen Profile

Antigen Summary

This gene is expressed in adipose tissue exclusively. It encodes a protein with similarity to collagens X and VIII and complement factor C1q. The encoded protein circulates in the plasma and is involved with metabolic and hormonal processes. Mutations in this gene are associated with adiponectin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified.

Alternative names and synonyms associated with Adiponectin (ADIPOQ)

  • adiponectin, C1Q and collagen domain containing (adipoq) Elisa Kit
  • adiponectin, C1Q and collagen domain containing (ADIPOQ) Elisa Kit
  • adiponectin (LOC100009027) Elisa Kit
  • adiponectin, C1Q and collagen domain containing (Adipoq) Elisa Kit
  • 30kDa Elisa Kit
  • Acdc Elisa Kit
  • Acrp30 Elisa Kit
  • adipo Elisa Kit
  • ADIPOQ Elisa Kit
  • ADIPQTL1 Elisa Kit
  • ADN Elisa Kit
  • ADPN Elisa Kit
  • APM-1 Elisa Kit
  • apM1 Elisa Kit
  • APN Elisa Kit
  • GBP28 Elisa Kit
  • MGC84292 Elisa Kit

Protein level used designations for ADIPOQ

adiponectin, C1Q and collagen domain containing , adiponectin , 30 kDa adipocyte complement-related protein , adipocyte complement-related 30 kDa protein , adipose most abundant gene transcript 1 protein , adipose specific collagen-like factor , gelatin-binding protein 28 , adipocyte complement related protein , adipocyte, C1Q and collagen domain containing , adipocyte, C1q and collagen domain-containing protein , adipocyte-specific protein AdipoQ , adipocyte complement related protein of 30 kDa , adipocyte complement related 30kDa protein , apM-1

444678 Xenopus laevis
471032 Pan troglodytes
554338 Felis catus
574212 Macaca mulatta
100009027 Oryctolagus cuniculus
9370 Homo sapiens
11450 Mus musculus
246253 Rattus norvegicus
403625 Canis lupus familiaris
397660 Sus scrofa
282865 Bos taurus
404536 Gallus gallus
100294598 Ovis aries
100735862 Cavia porcellus
101111848 Ovis aries
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