Sakura Tissue Tek Accu Edge Trimming Knife Blades Long 4789

Lab Reagents

Human IgG antibody Laboratories manufactures the sakura tissue tek accu edge trimming knife blades long 4789 reagents distributed by Genprice. The Sakura Tissue Tek Accu Edge Trimming Knife Blades Long 4789 reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact sakura tissue tek. Other Sakura products are available in stock. Specificity: Sakura Category: Tissue Group: Tek Accu

Tek Accu information

Anti-TEK antibody

STJ25807 100 µl
EUR 277
Description: This gene encodes a receptor that belongs to the protein tyrosine kinase Tie2 family. The encoded protein possesses a unique extracellular region that contains two immunoglobulin-like domains, three epidermal growth factor (EGF)-like domains and three fibronectin type III repeats. The ligand angiopoietin-1 binds to this receptor and mediates a signaling pathway that functions in embryonic vascular development. Mutations in this gene are associated with inherited venous malformations of the skin and mucous membranes. Alternative splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known.

Anti-TEK antibody

STJ29302 100 µl
EUR 277
Description: This gene encodes a receptor that belongs to the protein tyrosine kinase Tie2 family. The encoded protein possesses a unique extracellular region that contains two immunoglobulin-like domains, three epidermal growth factor (EGF)-like domains and three fibronectin type III repeats. The ligand angiopoietin-1 binds to this receptor and mediates a signaling pathway that functions in embryonic vascular development. Mutations in this gene are associated with inherited venous malformations of the skin and mucous membranes. Alternative splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known.

Anti-TEK Antibody

STJ503257 100 µg
EUR 476

Anti-TEK Antibody

STJ503258 100 µg
EUR 476

TEK Rabbit pAb

A0743-100ul 100 ul
EUR 308

TEK Rabbit pAb

A0743-200ul 200 ul
EUR 459

TEK Rabbit pAb

A0743-20ul 20 ul
EUR 183

TEK Rabbit pAb

A0743-50ul 50 ul
EUR 223

TEK Rabbit pAb

A7222-100ul 100 ul
EUR 308

TEK Rabbit pAb

A7222-200ul 200 ul
EUR 459

TEK Rabbit pAb

A7222-20ul 20 ul
EUR 183

TEK Rabbit pAb

A7222-50ul 50 ul
EUR 223

TEK Conjugated Antibody

C37274 100ul
EUR 397

Aldh3A2 Antibody

4789-002mg 0.02 mg
EUR 171.82
Description: Aldh3A2 Antibody: Aldh3A2 is a member of the aldehyde dehydrogenase superfamily, a group of NAD(P)(+)-dependent enzymes that catalyze the oxidation of a wide spectrum of aliphatic and aromatic aldehydes. Aldehyde dehydrogenase enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. Aldh3A2 catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acids. Mutations in the Aldh3A2 gene cause Sjogren-Larrson syndrome, an inherited neurocutaneous disorder. Patients with this disorder display ichthyosis, mental retardation and spastic diplegia. The pathogenesis of the cutaneous and neurological symptoms is thought to result from abnormal lipid accumulation in the membranes of skin and brain, the formation of aldehyde Schiff base adducts with amine-containing lipids or proteins, or defective eicosanoid metabolism.

Aldh3A2 Antibody

4789-01mg 0.1 mg
EUR 436.42
Description: Aldh3A2 Antibody: Aldh3A2 is a member of the aldehyde dehydrogenase superfamily, a group of NAD(P)(+)-dependent enzymes that catalyze the oxidation of a wide spectrum of aliphatic and aromatic aldehydes. Aldehyde dehydrogenase enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. Aldh3A2 catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acids. Mutations in the Aldh3A2 gene cause Sjogren-Larrson syndrome, an inherited neurocutaneous disorder. Patients with this disorder display ichthyosis, mental retardation and spastic diplegia. The pathogenesis of the cutaneous and neurological symptoms is thought to result from abnormal lipid accumulation in the membranes of skin and brain, the formation of aldehyde Schiff base adducts with amine-containing lipids or proteins, or defective eicosanoid metabolism.

Meis3 Blocking Peptide

33R-4789 100 ug
EUR 180
Description: A synthetic peptide for use as a blocking control in assays to test for specificity of Meis3 antibody, catalog no. 70R-8736

MCL1 antibody

10R-4789 100 ul
EUR 691
Description: Mouse monoclonal MCL1 antibody