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Catalog Number:
(10280-216)
Supplier:
Bioss
Description:
The inherited blindness associated protein, aryl hydrocarbon receptor interacting protein-like 1 (AIPL1), interacts with the cell cycle regulator protein NUB1. AIPL1 is crucial for protein folding and stabilization, as well as for protein trafficking. It localizes to the nucleus or cytoplasm and is highly expressed in the pineal gland and the retina. In the retina, AIPL1 is expressed in both developing cone and rod photoreceptors, but it is restricted to rod photoreceptors in the adult human retina. Defects in the gene encoding for AIPL1 can cause Leber congenital amaurosis type IV, an early-onset, inherited autosomal recessive disorder that results in childhood blindness.
Supplier:
Strem Chemicals Inc
Description:
CAS #: 13291-61-7. Size: 25g.
Catalog Number:
(68000-416)
Supplier:
Baxter
Description:
Ringer's sterile solutions for injection.
Supplier:
Spectrum Chemicals
Description:
(1,2-Cyclohexylenedinitrilo)tetraacetic Acid, Reagent is an alkyl-substituted amino acid that functions as a chelating agent. This ingredient's source is synthetic. It appears as a solid and is partially soluble in cold water. Its reagent grade means this is the highest quality commercially available for this chemical and that the American Chemical Society has not officially set any specifications for this material.
Supplier:
Envirco
Description:
These self-contained, laminar flow clean benches feature a modular design with an airflow pattern that offers the non-aspirating action of vertical flow while retaining the positive work protection of horizontal flow
Catalog Number:
(89290-444)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to SCN4B
Catalog Number:
(RL009-001-106)
Supplier:
Rockland Immunochemical
Description:
0.5mg. Protein Concentration: 1 mg/mL. Buffer: 0.5M acetic acid. Stabilizer: None. Preservative: 0.01% (w/v) sodium azide. For research. Sterile filtered liquid.
Catalog Number:
(10406-088)
Supplier:
Bioss
Description:
Defects in G6PD are the cause of chronic non-spherocytic hemolytic anemia (CNSHA) . Deficiency of G6PD is associated with hemolytic anemia in two different situations. First, in areas in which malaria has been endemic, G6PD-deficiency alleles have reached high frequencies (1% to 50%) and deficient individuals, though essentially asymptomatic in the steady state, have a high risk of acute hemolytic attacks. Secondly, sporadic cases of G6PD deficiency occur at a very low frequencies, and they usually present a more severe phenotype. Several types of CNSHA are recognized. Class-I variants are associated with severe NSHA; class-II have an activity <10% of normal; class-III have an activity of 10% to 60% of normal; class-IV have near normal activity.
Catalog Number:
(220022-948)
Supplier:
R&D Systems
Description:
The Recombinant Human Reg4 Protein from R&D Systems is derived from E. coli. The Recombinant Human Reg4 Protein has been validated for the following applications: Bioactivity.
Catalog Number:
(220019-039)
Supplier:
R&D Systems
Description:
Anti-REG4 Mouse Monoclonal Antibody [clone: 200214]
Catalog Number:
(RL600-406-108)
Supplier:
Rockland Immunochemical
Description:
Anti-Collagen Type VI (RABBIT) Antibody Biotin Conjugated is suitable for western blot, immunoprecipitatioin, and immunochemistry. Researchers should determine optimal titers for applications that are not stated below.
Catalog Number:
(10256-184)
Supplier:
Bioss
Description:
17Beta-HSD4 (17Beta-hydroxysteroid dehydrogenase type 4) is also known as peroxisomal multifunctional enzyme/protein 2 (MFE-2/MFP-2), D-bifunctional enzyme or 17-Beta Estradiol dehydrogenase type IV. It belongs to the 17Beta-HSD family of proteins that regulate the availability of steroids within various tissues throughout the body. 17Beta-HSD4 inactivates Estradiol through its oxidative activity but it is primarily involved in peroxisomal fatty acid and cholesterol Beta-oxidation. It has a multi-domain structure: the dehydrogenase domain is fused to a hydratase and a lipid transfer domain. 17Beta-HSD4 is a target protein of chromeceptin and it is essential for the downstream activation of Stat6. 17Beta-HSD4-deficient patients exhibit Zellweger-like syndrome and die within the first year of life. They display neuronal migration defects, facial dysmorphisms, severe hypotonia and convulsions in the neonatal period.
Catalog Number:
(76121-020)
Supplier:
Bioss
Description:
Phosphatidylinositol-glycan-specific phospholipase D (GPI-PLD) is a high-density lipoprotein-associated protein found on chromosome 6p22 that specifically hydrolyzes the inositol phosphate linkage in proteins anchored by phosphatidylinositol-glycans (PI-Gs). GPI-PLD is found in serum, liver, cerebrospinal fluid and in milk. The majority of plasma GPI-PLD appears to be specifically associated with a small, discrete and minor fraction of lipoproteins containing apoA-I and apoA-IV. Serum GPI-PLD activity is reduced over 75% in systemic inflammatory response syndrome and the downregulation of GPI-PLD could play an important role in the control of proinflammatory responses.
Catalog Number:
(10407-274)
Supplier:
Bioss
Description:
Shelters ceramides and diacylglycerol lipids inside its START domain and mediates the intracellular trafficking of ceramides and diacylglycerol lipids in a non-vesicular manner.
Catalog Number:
(89424-262)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to B4GALT5 (UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 5)
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
 is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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