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Description: Arylsulfatase F, also known as ARSF, is a 590 amino acid secretory protein that belongs to the sulfatase family of bone and cartilage matrix proteins. Arylsulfatase F uses calcium as a cofactor to catalyze reactions that are important in maintaining correct bone composition. The activity of Arylsulfatase F, unlike that of other family members, such as Arylsulfatase E, is not inhibited by warfarin. The gene encoding Arylsulfatase F maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.
Catalog Number: 76109-916
Supplier: Bioss


Description: Maintaining fluid integrity during fluid transfer is critical in numerous pharmaceutical and biotechnology applications.
Catalog Number: 89176-622
Supplier: Saint Gobain Life Sciences

Description: G-Biosciences' OmniPrep™ genomic DNA kits are for the extraction of ultra pure, high quality 100kb genomic DNA and are suitable for all downstream applications
Catalog Number: CA95029-212
Supplier: G-Biosciences


Description: Pack away detachable hood and elasticated storm cuffs.
Catalog Number: 76105-776
Supplier: Portwest


Description: Protect your pump, valves and other components in fluid line.
Catalog Number: MFLX30538-88
Supplier: VWR International


Description: Mechanical innovations reduce risk of fluid cross-over and contamination.
Catalog Number: MFLX40262-06
Supplier: VWR International

Description: Waterproof pants with sealed seams.
Catalog Number: 76105-292
Supplier: Portwest


Description: MLC1 is a 377 amino acid multi-pass membrane protein that may serve as a non-selective neuronal cation channel in brain. Mutant MLC1 proteins that show impaired folding have been corrected in vitro with the addition of a Ca(2+)-ATPase inhibitor, curcumin. Mutations in the gene encoding MLC1 is the cause of megalencephalic leukoencephalopathy with subcortical cysts, also known as van der Knaap disease, a rare syndrome characterized early in life by progressive brain destruction causing mental retardation and incoordination. Single nucleotide polymorphisms within the MLC1 gene may be associated with periodic catatonia, but there seems to be conflicting evidence on whether or not the gene is implicated in general schizophrenia.
Catalog Number: 10462-050
Supplier: Bioss


Description: Wheaton lab 45 media bottles are manufactured from USP Type I borosilicate glass.
Catalog Number: 15507-102
Supplier: DWK Life Sciences (KIMBLE)

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Description: Cotton comfort long sleeve T-shirts are manufactured from a moisture wicking fabric that helps to keep the body dry.
Catalog Number: 76105-284
Supplier: Portwest


Description: Arylsulfatase F, also known as ARSF, is a 590 amino acid secretory protein that belongs to the sulfatase family of bone and cartilage matrix proteins. Arylsulfatase F uses calcium as a cofactor to catalyze reactions that are important in maintaining correct bone composition. The activity of Arylsulfatase F, unlike that of other family members, such as Arylsulfatase E, is not inhibited by warfarin. The gene encoding Arylsulfatase F maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.
Catalog Number: 10667-096
Supplier: Bioss


Description: MLC1 is a 377 amino acid multi-pass membrane protein that may serve as a non-selective neuronal cation channel in brain. Mutant MLC1 proteins that show impaired folding have been corrected <i>in vitro</i> with the addition of a Ca(2+)-ATPase inhibitor, curcumin. Mutations in the gene encoding MLC1 is the cause of megalencephalic leukoencephalopathy with subcortical cysts, also known as van der Knaap disease, a rare syndrome characterized early in life by progressive brain destruction causing mental retardation and incoordination. Single nucleotide polymorphisms within the MLC1 gene may be associated with periodic catatonia, but there seems to be conflicting evidence on whether or not the gene is implicated in general schizophrenia.
Catalog Number: 76119-264
Supplier: Bioss


Description: Arylsulfatase F, also known as ARSF, is a 590 amino acid secretory protein that belongs to the sulfatase family of bone and cartilage matrix proteins. Arylsulfatase F uses calcium as a cofactor to catalyze reactions that are important in maintaining correct bone composition. The activity of Arylsulfatase F, unlike that of other family members, such as Arylsulfatase E, is not inhibited by warfarin. The gene encoding Arylsulfatase F maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.
Catalog Number: 10667-098
Supplier: Bioss


Description: Mechanical innovations reduce risk of fluid cross-over and contamination.
Catalog Number: MFLX40261-06
Supplier: VWR International

Description: Neurofilament Marker (pan-neuronal, cocktail), Monoclonal antibody, Clone: SMI 311, Host: Mouse, Species reactivity: Mammalian, Isotype: IgG1 and IgM Cocktail, Formulation: Ascites Fluid (contains 0.01M sodium azide), Application: IHC, WB, ELISA, Size: 100 ul
Catalog Number: CA10818-032
Supplier: Biolegend


Description: Protect your pump, valves and other components in fluid line.
Catalog Number: MFLX30536-22
Supplier: VWR International


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