108 Results for: "2,3-Dichlorophenyl isothiocyanate&amp"

Supplier: Thermo Fisher Scientific

2,3-Dichlorophenyl isothiocyanate ≥97%

Supplier: Apollo Scientific

2,3-Dichlorophenyl isothiocyanate 97%

Supplier: TCI

2,3-Dichlorophenyl isothiocyanate ≥98.0% (by GC)

Supplier: Thermo Scientific

2,3-Dichlorophenyl isothiocyanate

Supplier: Apollo Scientific

3,4-Dichlorophenyl isothiocyanate

Supplier: Apollo Scientific

2,6-Dichlorophenyl isothiocyanate

Supplier: Thermo Fisher Scientific

2,6-Dichlorophenyl isothiocyanate ≥98%

Supplier: Thermo Fisher Scientific

2,4-Dichlorophenyl isothiocyanate ≥97%

Supplier: TCI

3,4-Dichlorophenyl isothiocyanate ≥98.0% (by GC)

Supplier: TCI

2,4-Dichlorophenyl isothiocyanate ≥98.0% (by GC)

Supplier: Thermo Scientific

3,4-Dichlorophenyl isothiocyanate

Supplier: Thermo Scientific

2,5-Dichlorophenyl isothiocyanate

Supplier: Thermo Scientific

2,4-Dichlorophenyl isothiocyanate

Supplier: Apollo Scientific

2,3-Difluorophenyl isothiocyanate 95%

Supplier: Apollo Scientific

6-Isothiocyanato-2,3-dihydro-1,4-benzodioxine 95%

Supplier: Apollo Scientific

4-Isothiocyanato-2-(trifluoromethyl)benzonitrile

Supplier: Apollo Scientific

2-Isothiocyanatobicyclo[2.2.1]heptane

Supplier: Bioss

The claudin superfamily consists of structurally related proteins that are important structural and functional components of tight junctions. Claudin-23, also known as CLDN23 or CLDNL, is a 292 amino acid multi-pass membrane protein that localizes to cell junctions and belongs to the claudin family. Expressed in stomach and placenta, as well as in germinal center B-cells, claudin-23 is thought to exhibit calcium-dependent cell-adhesion activity through which it plays an essential role in tight junction-specific obliteration of the intercellular space. Human claudin-23 shares 80% sequence similarity with its mouse counterpart, suggesting a conserved role between species. Overexpression of claudin-23 is associated with colon tumors, implicating claudin-23 as a possible metastasis factor.

Supplier: TCI

4-Isothiocyanato-2-(trifluoromethyl)benzonitrile ≥98.0% (by GC)

Supplier: ENZO LIFE SCIENCES

Rifampicin

Supplier: Bioss

Associates with IL12B to form the IL-23 interleukin, a heterodimeric cytokine which functions in innate and adaptive immunity. IL-23 may constitute with IL-17 an acute response to infection in peripheral tissues. IL-23 binds to a heterodimeric receptor complex composed of IL12RB1 and IL23R, activates the Jak-Stat signaling cascade, stimulates memory rather than naive T-cells and promotes production of proinflammatory cytokines. IL-23 induces autoimmune inflammation and thus may be responsible for autoimmune inflammatory diseases and may be important for tumorigenesis.

Supplier: Bioss

Adhesion molecule in postnatal neural development that mediates sialic-acid dependent cell-cell interactions between neuronal and myelinating cells. Preferentially binds to alpha-2,3-linked sialic acid (By similarity).

Supplier: Bioss

Adhesion molecule in postnatal neural development that mediates sialic-acid dependent cell-cell interactions between neuronal and myelinating cells. Preferentially binds to alpha-2,3-linked sialic acid (By similarity).

Supplier: TCI

Rifampicin ≥98.0% (by titrimetric analysis)

Supplier: Thermo Fisher Scientific

Rifampicin 95%

Supplier: Bioss

Has a role in maintaining calcium homeostasis. Catalyzes the NADPH-dependent 24-hydroxylation of calcidiol (25-hydroxyvitamin D(3)) and calcitriol (1-alpha,25-dihydroxyvitamin D(3)). The enzyme can perform up to 6 rounds of hydroxylation of calcitriol leading to calcitroic acid. It also shows 23-hydroxylating activity leading to 1-alpha,25-dihydroxyvitamin D(3)-26,23-lactone as end product.

Supplier: Bioss

BPGM (2,3-bisphosphoglycerate mutase) is a 259 amino acid protein that belongs to the phosphoglycerate mutase family and exists as a homodimer that plays a crucial role in the regulation of hemoglobin oxygen. Specifically, BPGM catalyzes the conversion of 3-D-glyceroyl phosphate to 2,3-bisD-glycerate (2,3-BPG), a reaction that is essential for controlling the concentration of 2,3-BPG within the cell. The gene encoding BPGM maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Involvement in disease:Defects in BPGM are the cause of bisphosphoglycerate mutase deficiency (BPGMD) . A disease characterized by hemolytic anemia, splenomegaly, cholelithiasis and cholecystitis.

Supplier: Bioss

Functions as an interleukin receptor which binds interleukin-12 with low affinity and is involved in IL12 transduction. Associated with IL12RB2 it forms a functional, high affinity receptor for IL12. Associates also with IL23R to form the interleukin-23 receptor which functions in IL23 signal transduction probably through activation of the Jak-Stat signaling cascade.

Supplier: Bioss

Displays NADPH-dependent dicarbonyl reductase activity in vitro with 3,4-Hexanedione, 2,3-Heptanedione and 1-Phenyl-1,2-propanedione as substrates. No reductase activity is displayed in vitro with steroids, retinoids and sugars as substrates. Attenuates MDM2-mediated p53/TP53 degradation, leading to p53/TP53 stabilization and increased transcription activity, resulting in the accumulation of MDM2 and CDKN1A/p21.

Supplier: Thermo Scientific

2,3-Xylyl isothiocyanate