Tributyl(ethyl)phosphonium+Diethyl+Phosphate
Catalog Number:
(89366-424)
Supplier:
Genetex
Description:
Rabbit polyclonal to Sphingolipid Receptor Edg3/S1P3
Catalog Number:
(10099-970)
Supplier:
Prosci
Description:
POLK belongs to the DNA polymerase type-Y family. It contains 2 Rad18-type zinc fingers and 1 umuC domain. POLK is a DNA polymerase specifically involved in DNA repair. It plays an important role in translesion synthesis, where the normal high-fidelity DNA polymerases cannot proceed and DNA synthesis stalls. Depending on the context, it inserts the correct base, but causes frequent base transitions, transversions and frameshifts. It lacks 3'-5' proofreading exonuclease activity. POLK forms a Schiff base with 5'-deoxyribose phosphate at abasic sites, but does not have lyase activity.
Catalog Number:
(10756-378)
Supplier:
Biolegend
Description:
Purified anti-mouse FcεRIα (MaxPar® Ready) [MAR-1]; Isotype: Armenian Hamster IgG; Reactivity: Mouse; Apps: FC, CyTOF®; Size: 100 μg
Catalog Number:
(89270-596)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to RTCD1 (N-terminal)
Catalog Number:
(89366-420)
Supplier:
Genetex
Description:
Rabbit polyclonal to Sphingolipid Receptor Edg1/S1P1
Catalog Number:
(10757-108)
Supplier:
Biolegend
Description:
Brilliant Violet 570™ anti-human CD3 [UCHT1]; Isotype: Mouse IgG1, κ; Reactivity: Human, Cross-Reactivity: Chimpanzee; Apps: FC; Size: 100 tests
Catalog Number:
(76085-502)
Supplier:
Bioss
Description:
Catalyzes the hydrolysis of fructose 1,6-bisphosphate to fructose 6-phosphate in the presence of divalent cations, acting as a rate-limiting enzyme in gluconeogenesis. Plays a role in regulating glucose sensing and insulin secretion of pancreatic beta-cells. Appears to modulate glycerol gluconeogenesis in liver. Important regulator of appetite and adiposity; increased expression of the protein in liver after nutrient excess increases circulating satiety hormones and reduces appetite-stimulating neuropeptides and thus seems to provide a feedback mechanism to limit weight gain.
Catalog Number:
(89298-046)
Supplier:
Genetex
Description:
Goat polyclonal antibody to GAPDH (C Terminus)
Catalog Number:
(89267-610)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to PIP5KL1 (Middle)
Catalog Number:
(10353-048)
Supplier:
Bioss
Description:
Inhibitor of protein-phosphatase 1.
Catalog Number:
(10389-578)
Supplier:
Bioss
Description:
CYP2R1 is a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are mono-oxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This enzyme is a microsomal vitamin D hydroxylase that converts vitamin D into the active ligand for the vitamin D receptor.Defects in CYP2R1 are a cause of 25-hydroxyvitamin D(3) deficiency, also known as pseudovitamin D(3) deficiency rickets due to 25-hydroxylase deficiency. First described in patients who had rickets at a young age despite a history of adequate vitamin D intake. The patients sera had low calcium concentrations, low phosphate concentrations, elevated alkaline phosphatase activity and low levels of 25-hydroxyvitamin D.
Catalog Number:
(10164-982)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to SPP24
Catalog Number:
(MKV55310)
Supplier:
AVANTOR PERFORMANCE MATERIALS US
Description:
Ethyl acetate ≥99.6%, AR® for liquid chromatography, for UV spectrophotometry, Macron Fine Chemicals™
Catalog Number:
(89270-130)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to GFPT2 (Middle)
Catalog Number:
(89292-330)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to CI-MPR
Catalog Number:
(10748-722)
Supplier:
Prosci
Description:
LIMP2 Antibody: The lysosomal integral membrane protein 2 (LIMP2) is a heavily glycosylated type III transmembrane protein, the majority of which exists in the lumen of the lysosome and a cytoplasmic domain of approximately 20 amino acids. A deficiency of LIMP2 in mice causes uretic pelvic junction obstruction, deafness, and peripheral neuropathy associated with impaired vesicular trafficking and distribution of apically expressed proteins. More recently, LIMP2 was shown to act as a receptor to bind beta-glucocerebrosidase, the enzyme defective in Gaucher disease, a lysosomal storage disorder. LIMP2-deficient mice showed missorted as well as secreted beta-glucocerebrosidase, suggesting that LIMP2 also functions as the mannose-6-phosphate-independent trafficking receptor.
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