Tissue Lysates
Cayman Chemical PTK7 EXrAClular DomaInhu 100ug
Source: Recombinant human C-terminal His-tagged PTK7 extracellular domain expressed in HEK293 cells • Amino acids: 1-704 • MW: 76.1 kDa
Cayman Chemical 11 12EETd11 methyl este 100ug
An internal standard for the quantification of 11(12)-EET methyl ester by GC- or LC-MS
Cayman Chemical 11S 12R-EET 100UG
An oxylipin and a metabolite of arachidonic acid; activates KCa1.1/BK in isolated rat coronary small arterial smooth muscle cells at 50 nM; induces dilation of precontracted isolated canine epicardial arterioles (EC50 = 20 pM) and denuded porcine subepicardial arterioles (EC50 = 10 pM)
Cayman Chemical IgG4humn Monclonal ntIb 100ug
Immunogen: Peptide corresponding to the hinge region of human IgG4 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Human IgG4; (-) Human IgG1, IgG2, IgG3, IgM, IgA, IgD, IgE; (-) Cynomolgus monkey, goat, mouse, rat, or rhesus monkey IgG • Applications: ELISA, FC, ICC, IHC, WB • MW = 150 and 50 kDa for whole IgG4 and the IgG4 heavy chain under non-reducing and reducing conditions, respectively
Cayman Chemical OsteocalcIn1-49humnt 100ug
A bone peptide; secreted by osteoblasts and odontoblasts and comprises 1-2% of the total protein in bone; plasma levels increase in diseases that induce dysregulated bone turnover; positively correlated with insulin sensitivity and negatively correlated with high blood glucose levels in women; induces chemotaxis of MDA-MB-231 breast cancer cells, human peripheral blood monocytes, and rat osteosarcoma cells with osteoblast-like characteristics; positively associated with calcification of aortic tissue and heart valves in humans
Cayman Chemical HGFhumnrecombInt 100ug
Source: Active recombinant human HGF expressed in CHO cells • Amino acids: 32-728 • MW: 79.7 kDa
ABclonal Technology Thyroid peroxidase/TPO
This gene encodes a membrane-bound glycoprotein The encoded protein acts as an enzyme and plays a central role in thyroid gland function The protein functions in the iodination of tyrosine residues in thyroglobulin and phenoxy-ester formation between pairs of iodinated tyrosines to generate the thyroid hormones thyroxine and triiodothyronine Mutations in this gene are associated with several disorders of thyroid hormonogenesis including congenital hypothyroidism congenital goiter and thyroid hormone organification defect IIA Multiple transcript variants encoding distinct isoforms have been identified for this gene but the full-length nature of some variants has not been determined