Troponin T, Slow Skeletal Muscle (TNNI1) ELISA试剂盒

TNNI1 encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. 再加上,我们可以发TNNI1 抗体 (50)TNNI1 蛋白 (13)和数多这个蛋白质的别的产品。

list all ELISA KIts 基因 基因ID UniProt
TNNI1 7138 P13805
TNNI1 21955 O88346
TNNI1 171409 Q7TNB2
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产品编号 适用 灵敏度 范围 图像 规格 供应商 交付 价格 详细
5.5 pg/mL 15.6 pg/mL - 1000 pg/mL 96 Tests Log in to see 13至16个工作日
$589.47
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Pig 7.8 pg/mL 31.25-2000 pg/mL Typical standard curve 96 Tests Log in to see 15至18个工作日
$1,026.67
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小鼠 5.8 pg/mL 15.62 pg/mL - 1000 pg/mL 96 Tests Log in to see 13至16个工作日
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大鼠 5.2 pg/mL 15.62 pg/mL - 1000 pg/mL 96 Tests Log in to see 13至16个工作日
$640.00
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Cow 3.13 pg/mL   96 Tests Log in to see 15至18个工作日
$1,026.67
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小鸡 37.5 pg/mL 62.5-4000 pg/mL   96 Tests Log in to see 12至14个工作日
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0.094 ng/mL 0.156-10 ng/mL   96 Tests Log in to see 12至14个工作日
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9.375 pg/mL 15.625-1000 pg/mL   96 Tests Log in to see 12至14个工作日
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4.688 pg/mL 7.813 pg/mL - 500 pg/mL   96 Tests Log in to see 12至14个工作日
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引用最多的TNNI1 ELISA试剂盒

  1. Human TNNI1 ELISA Kit for Sandwich ELISA - ABIN418922 : King, Abreu, Cheng, Chertoff, Brotto, Kelly, Brotto: A multimodal assessment of balance in elderly and young adults. in Oncotarget 2016 (PubMed)

适于 TNNI1 相互作用对的更多 ELISA 试剂盒

Human Troponin T, Slow Skeletal Muscle (TNNI1) interaction partners

  1. This study describes the first TNNT1 mutation that transmits in an autosomal dominant fashion to cause nemaline myopathy.

  2. investigated the effects of one of these mutations, K247R of TnT, on the picosecond dynamics of the Tn core domain (Tn-CD), consisting of TnC (显示 TNC ELISA试剂盒), TnI (显示 TNNI2 ELISA试剂盒) and TnT2 (183-288 residues of TnT), by carrying out the quasielastic neutron scattering measurements on the reconstituted Tn-CD containing either the wild-type TnT2 (wtTn-CD) or the mutant TnT2 (K247R-Tn-CD) in the absence and presence of Ca(2 (显示 CA2 ELISA试剂盒)+)

  3. Data suggest that mutations in troponin C (TnC, A8V) and troponin T (TnT, delta14-TnT) found in patients with hypertrophic cardiomyopathy together fully stabilize the active M state of regulated actin (the actin-tropomyosin-troponin complex).

  4. pathogenesis of TNNT1 myopathies

  5. Copeptin (显示 AVP ELISA试剂盒) and troponin T measurement could potentially improve the prehospital diagnostic and prognostic classification of patients with a suspected AMI (显示 CFD ELISA试剂盒).

  6. TNNT1 genetic and epigenetic variations are associated with HDL (显示 HSD11B1 ELISA试剂盒)-C levels and coronary artery disease.

  7. Three homologous genes have evolved in vertebrates to encode three muscle type-specific TnT isoforms: TNNT1 for slow skeletal muscle TnT, TNNT2 for cardiac muscle TnT, and TNNT3 for fast skeletal muscle TnT.

  8. Nemaline body myopathy Palestinian patients were found to have a novel mutation in troponin T1.

  9. troponin T and creatinine kinase isoenzyme (CK-MB) have roles in combined renal and myocardial injuries in asphyxiated infants

  10. Biopsy-proven acute and viral myocarditis is associated with elevated concentrations of hs-TnT.

Mouse (Murine) Troponin T, Slow Skeletal Muscle (TNNI1) interaction partners

  1. Mouse tumor endothelial cells express troponin T.

  2. demonstrated that ssTnT deficiency resulted in significantly decreased levels of other slow fibre-specific myofilament proteins whereas fast fibre-specific myofilament proteins were increased correspondingly

  3. the induction of Tnnt1 gene expression in adult mouse brains by ketamine may illustrate the genes involved in the metabolic syndromes observed in neuropsychiatric disorders

  4. Data show that cardiac expression of slow skeletal troponin T (Tnnt1) strictly depends on the physical interaction between GATA4-FOG2 in the myocardium of both atria and ventricles.

TNNI1 抗原简介

Antigen Summary

This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with TNNI1

  • troponin T1, slow skeletal type (TNNT1) 抗体
  • troponin I, slow skeletal muscle (tnni1) 抗体
  • troponin I1, slow skeletal type (TNNI1) 抗体
  • troponin I type 1 (skeletal, slow) (tnni1) 抗体
  • troponin T1, skeletal, slow (Tnnt1) 抗体
  • troponin T1, slow skeletal type (Tnnt1) 抗体
  • troponin T1, slow skeletal type S homeolog (tnnt1.S) 抗体
  • troponin T type 1 (skeletal, slow) (tnnt1) 抗体
  • ANM 抗体
  • AW146156 抗体
  • Fang2 抗体
  • MGC75706 抗体
  • NEM5 抗体
  • ssTnT 抗体
  • sTnT 抗体
  • TNNI1 抗体
  • Tnnt 抗体
  • Tnt 抗体
  • tnTs 抗体
  • zgc:193831 抗体
  • zgc:193865 抗体

Protein level used designations for TNNI1

nemaline myopathy type 5 , slow skeletal muscle troponin T , troponin T, slow skeletal muscle , troponin-T1, skeletal, slow , troponin I, skeletal, slow , troponin I type 1 (skeletal, slow) , troponin I, skeletal, slow 1 , sTnT , tnTs , troponin T1, skeletal, slow , troponin T slow type isoform sTnT1 , skeletal muscle slow-twitch TnT

GENE ID SPECIES
7138 Homo sapiens
100196284 Salmo salar
469636 Pan troglodytes
394556 Xenopus (Silurana) tropicalis
282095 Bos taurus
396579 Sus scrofa
21955 Mus musculus
171409 Rattus norvegicus
444636 Xenopus laevis
558627 Danio rerio
100720501 Cavia porcellus
476383 Canis lupus familiaris
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