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Catalog Number: (76101-092)
Supplier: Bioss
Description: Involved in oxygen transport in the brain. Hexacoordinate globin, displaying competitive binding of oxygen or the distal His residue to the iron atom. Not capable of penetrating cell membranes. The deoxygenated form exhibits nitrite reductase activity inhibiting cellular respiration via NO-binding to cytochrome c oxidase. Involved in neuroprotection during oxidative stress. May exert its anti-apoptotic activity by acting to reset the trigger level of mitochondrial cytochrome c release necessary to commit the cells to apoptosis.


Supplier: Gawet
Description: The 7.6 cm (3") thick marble slab construction provides maximum damping effect and vibration-free stability for analytical instrument scales.

Supplier: Thermo Scientific Chemicals
Description: Sodium tellurite is an intermediate in the extraction of the element, tellurium; it is a product obtained from anode slimes and is a precursor to tellurium. Solutions of sodium tellurite are used for black or blue-black coatings on iron, steel, aluminum, and copper.
Catalog Number: (10395-184)
Supplier: Bioss
Description: 12 Lipoxygenase is a non heme iron containing dioxygenase which stereospecifically incorporates molecular oxygen into cis,cis-1,4-pentadiene containing polyunsaturated fatty acids. Murine leukocyte 12 Lipoxygenase oxidizes arachidonic acid to 12(S)-HpETE and 15(S)-HpETE in a ratio of 3:1. Murine leukocyte 12 Lipoxygenase is a 75 kDa protein which is 58% homologous to murine platelet 12 Lipoxygenase, and 70% homologous to porcine leukocyte 12 Lipoxygenase.


Supplier: Thermo Fisher Scientific
Description: Orion™ AQUAfast Tablet Reagents perform colorimetric measurements of common water parameters with convenient, rapidly dissolving tablets.

Supplier: Thermo Scientific Chemicals
Description: Ferrozine mono-sodium salt hydrate 97%
Catalog Number: (470356-686)
Supplier: COOK IRON STORE
Description: Steel wool of size 00.

New Product


Catalog Number: (CA1.16982.0001)
Supplier: MilliporeSigma
Description: MilliporeSigma # 1.16128.0001 replaces and is identical to MilliporeSigma # 16128-1.
MilliporeSigma # 1.16720.0001 replaces and is identical to MilliporeSigma # 16720-1.
MilliporeSigma # 1.16957.0001 replaces and is identical to MilliporeSigma # 1.16957.0007.
MilliporeSigma # 1.16973.0001 replaces and is identical to MilliporeSigma # 16973-1.
MilliporeSigma # 1.16974.0001 replaces and is identical to MilliporeSigma # 16974-1.
MilliporeSigma # 1.16975.0001 replaces and is identical to MilliporeSigma # 16975-1.
MilliporeSigma # 1.16976.0001 replaces and is identical to MilliporeSigma # 16976-1.
MilliporeSigma # 1.16982.0001 replaces and is identical to MilliporeSigma # 16982-1.
MilliporeSigma # 1.16995.0001 replaces and is identical to MilliporeSigma # 16995-1.

Catalog Number: (CA90004-052)
Supplier: BD
Description: Differential medium to detect organisms that decarboxylate or deaminate lysine and produce hydrogen sulfide.

Catalog Number: (10483-774)
Supplier: Bioss
Description: OGFOD2


Catalog Number: (75790-230)
Supplier: Prosci
Description: Superoxide Dismutase (SOD2) belongs to the iron/manganese superoxide dismutase family. SOD2 is a mitochondrial matrix protein that forms a homotetramer and binds one manganese ion per subunit. SOD2 transforms toxic superoxide, a byproduct of the mitochondrial electron transport chain into hydrogen peroxide and diatomic oxygen. It is reported that oxidative stress plays an essential role in the development of breast cancer, while SOD2 is one of the primary enzymes that directly convert potential harmful oxidizing species to harmless metabolites.


Catalog Number: (470163-090)
Supplier: Ward's Science
Description: Determine The Equilibrium Constant for Colored Species

SDS


Catalog Number: (75784-552)
Supplier: Diversified Woodcrafts
Description: This sturdy vise is a swivel base vise and is ideal for the Robotics Bench.


Catalog Number: (76099-998)
Supplier: Bioss
Description: HGD is a 445 amino acid protein that belongs to the homogentisate dioxygenase family and is involved in the pathway of amino acid degradation. Expressed at high levels in kidney, colon, liver, prostate and small intestine, HGD uses iron as a cofactor to catalyze the oxygen-dependent conversion of homogentisate to 4-maleylacetoacetate, a reaction that is the fourth step in the creation of L-phenylalanine from fumarate and acetoacetic acid. Defects in the gene encoding HGD are the cause of alkaptonuria (AKU), an autosomal recessive disorder that is characterized by urine that turns dark on standing and alkalinization, black ochronotic pigmentation of cartilage and collagenous tissues and spine arthritis.


Catalog Number: (470311-148)
Supplier: Klinger
Description: This model is hand made in the USA by Klinger Educational Products.


Catalog Number: (10481-994)
Supplier: Bioss
Description: Defects in PANK2 are the cause of neurodegeneration with brain iron accumulation type 1 (NBIA1); also known as pantothenate kinase-associated neurodegeneration (PKAN) or Hallervorden-Spatz syndrome (HSS). It is an autosomal recessive neurodegenerative disorder associated with iron accumulation in the brain, primarily in the basal ganglia. Clinical manifestations include progressive muscle spasticity, hyperreflexia, muscle rigidity, dystonia, dysarthria, and intellectual deterioration which progresses to severe dementia over several years. It is clinically classified into classic, atypical, and intermediate phenotypes. Classic forms present with onset in the first decade, rapid progression, loss of independent ambulation within 15 years. Atypical forms have onset in the second decade, slow progression, maintenance of independent ambulation up to 40 years later. Intermediate forms manifest onset in the first decade with slow progression or onset in the second decade with rapid progression. Patients with early onset tend to also develop pigmentary retinopathy, whereas those with later onset tend to also have speech disorders and psychiatric features. All patients have the 'eye of the tiger' sign on brain MRI.Defects in PANK2 are the cause of hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP). HARP is a rare syndrome with many clinical similarities to NBIA1.


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