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Product Image-89160-374

Sodium dodecyl sulfate (SDS)

Catalog Number: (89160-374)
Supplier: Enzo Life Sciences
Description: Component of the 20S proteasome drug discovery assay.
Image Unavailable-TCP0302-025G

Dimethyl phthalate ≥99.0%

Supplier: TCI America
Description: CAS Number: 131-11-3
MDL Number: MFCD00008425
Molecular Formula: C10H10O4
Molecular Weight: 194.19
Purity/Analysis Method: >99.0% (GC)
Form: Clear Liquid
Boiling point (°C): 284
Flash Point (°C): 156
Freezing point (°C): 0
Specific Gravity (20/20): 1.19

SDS Certificates

Product Image-CAPI26125

Pierce™ CA(PEG)n Carboxy-PEG-Amine Compound, Thermo Scientific

Supplier: Thermo Scientific
Description: The carboxy-PEG<sub>n</sub>-amine (CA[PEG]n) PEGylation reagents are zwitterionic, amino acid derivatives that are used for modifying proteins or surfaces such as beads, nanoparticles and self-assembled monolayers

SDS Certificates

Image Unavailable-89514-326

Anti-HIST2H2BE Rabbit Polyclonal Antibody

Catalog Number: (89514-326)
Supplier: Abgent
Description: LEAF (Low Endotoxin, Azide-Free)
Image Unavailable-89513-062

Anti-PTF1A Rabbit Polyclonal Antibody

Catalog Number: (89513-062)
Supplier: Abgent
Description: Western Blot: 1:1000, Immunhistochemsitry: 1:10~50,
Image Unavailable-CA1.08677.0001

Xylenol orange tetrasodium salt indicator for metal titration, Supelco®

Supplier: MilliporeSigma
Description: Grade Acs,Reagent Ph Eur, Cas Number 3618-43-7, Metal Indicator

Certificates

Image Unavailable-10490-696

Anti-DYRK3 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (10490-696)
Supplier: Bioss
Description: Dyrk (for dual specificity tyrosine phosphorylation regulated kinase) is the homolog of the Drosophila mnb (minibrain) gene, which is required for neurogenesis. Dyrk is a dual-specificity tyrosine kinase and serine/threonine kinase, which is itself regulated by tyrosine phosphorylation. Several mammalian Dyrk related proteins have been identified and are thought to compose a family of dual specificity protein kinases. Dyrk family members, including Dyrk1A (originally Dyrk), Dyrk1B, Dyrk1C, Dyrk2, Dyrk3, Dyrk4A and Dyrk4B, are thought to be involved in diverse cellular functions. Two isoforms of human fetal brain Dyrk2 exist: a deduced 528-amino acid protein and a protein containing 73 additional amino acids at the amino terminus. Dyrk3 is strongly expressed in testis, only after the onset of spermatogenesis, and very weakly expressed in spleen and adrenal gland. The genes which encode Dyrk2 and Dyrk3 map to human chromosomes 12 and 1q32, respectively.
Image Unavailable-89516-876

Anti-GPATCH11 Rabbit Polyclonal Antibody

Catalog Number: (89516-876)
Supplier: Abgent
Description: Western Blot: 1:1000
Image Unavailable-10162-766

Anti-Pan-Ras Rabbit Polyclonal Antibody

Catalog Number: (10162-766)
Supplier: Genetex
Description: Rabbit polyclonal to Pan-Ras Asp12
Image Unavailable-10435-232

Anti-SMPD1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10435-232)
Supplier: Bioss
Description: Converts sphingomyelin to ceramide. Also has phospholipase C activities toward 1,2-diacylglycerolphosphocholine and 1,2-diacylglycerolphosphoglycerol. Isoform 2 and isoform 3 have lost catalytic activity.Involvement in disease: Defects in SMPD1 are the cause of Niemann-Pick disease type A (NPDA) ; also known as Niemann-Pick disease classical infantile form. It is an early-onset lysosomal storage disorder caused by failure to hydrolyze sphingomyelin to ceramide. It results in the accumulation of sphingomyelin and other metabolically related lipids in reticuloendothelial and other cell types throughout the body, leading to cell death. Niemann-Pick disease type A is a primarily neurodegenerative disorder characterized by onset within the first year of life, mental retardation, digestive disorders, failure to thrive, major hepatosplenomegaly, and severe neurologic symptoms. The severe neurological disorders and pulmonary infections lead to an early death, often around the age of four. Clinical features are variable. A phenotypic continuum exists between type A (basic neurovisceral) and type B (purely visceral) forms of Niemann-Pick disease, and the intermediate types encompass a cluster of variants combining clinical features of both types A and B.
Image Unavailable-10435-226

Anti-SMPD1 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10435-226)
Supplier: Bioss
Description: Converts sphingomyelin to ceramide. Also has phospholipase C activities toward 1,2-diacylglycerolphosphocholine and 1,2-diacylglycerolphosphoglycerol. Isoform 2 and isoform 3 have lost catalytic activity.Involvement in disease: Defects in SMPD1 are the cause of Niemann-Pick disease type A (NPDA) ; also known as Niemann-Pick disease classical infantile form. It is an early-onset lysosomal storage disorder caused by failure to hydrolyze sphingomyelin to ceramide. It results in the accumulation of sphingomyelin and other metabolically related lipids in reticuloendothelial and other cell types throughout the body, leading to cell death. Niemann-Pick disease type A is a primarily neurodegenerative disorder characterized by onset within the first year of life, mental retardation, digestive disorders, failure to thrive, major hepatosplenomegaly, and severe neurologic symptoms. The severe neurological disorders and pulmonary infections lead to an early death, often around the age of four. Clinical features are variable. A phenotypic continuum exists between type A (basic neurovisceral) and type B (purely visceral) forms of Niemann-Pick disease, and the intermediate types encompass a cluster of variants combining clinical features of both types A and B.
Image Unavailable-10490-702

Anti-DYRK3 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10490-702)
Supplier: Bioss
Description: Dyrk (for dual specificity tyrosine phosphorylation regulated kinase) is the homolog of the Drosophila mnb (minibrain) gene, which is required for neurogenesis. Dyrk is a dual-specificity tyrosine kinase and serine/threonine kinase, which is itself regulated by tyrosine phosphorylation. Several mammalian Dyrk related proteins have been identified and are thought to compose a family of dual specificity protein kinases. Dyrk family members, including Dyrk1A (originally Dyrk), Dyrk1B, Dyrk1C, Dyrk2, Dyrk3, Dyrk4A and Dyrk4B, are thought to be involved in diverse cellular functions. Two isoforms of human fetal brain Dyrk2 exist: a deduced 528-amino acid protein and a protein containing 73 additional amino acids at the amino terminus. Dyrk3 is strongly expressed in testis, only after the onset of spermatogenesis, and very weakly expressed in spleen and adrenal gland. The genes which encode Dyrk2 and Dyrk3 map to human chromosomes 12 and 1q32, respectively.
Image Unavailable-10435-234

Anti-SMPD1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10435-234)
Supplier: Bioss
Description: Converts sphingomyelin to ceramide. Also has phospholipase C activities toward 1,2-diacylglycerolphosphocholine and 1,2-diacylglycerolphosphoglycerol. Isoform 2 and isoform 3 have lost catalytic activity.Involvement in disease: Defects in SMPD1 are the cause of Niemann-Pick disease type A (NPDA) ; also known as Niemann-Pick disease classical infantile form. It is an early-onset lysosomal storage disorder caused by failure to hydrolyze sphingomyelin to ceramide. It results in the accumulation of sphingomyelin and other metabolically related lipids in reticuloendothelial and other cell types throughout the body, leading to cell death. Niemann-Pick disease type A is a primarily neurodegenerative disorder characterized by onset within the first year of life, mental retardation, digestive disorders, failure to thrive, major hepatosplenomegaly, and severe neurologic symptoms. The severe neurological disorders and pulmonary infections lead to an early death, often around the age of four. Clinical features are variable. A phenotypic continuum exists between type A (basic neurovisceral) and type B (purely visceral) forms of Niemann-Pick disease, and the intermediate types encompass a cluster of variants combining clinical features of both types A and B.
Product Image-10108-518

Anti-WDR12 Rabbit Polyclonal Antibody

Catalog Number: (10108-518)
Supplier: Prosci
Description: WDR12 is a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. The function of this protein is not known.This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein is highly similar to the mouse WD repeat domain 12 protein at the amino acid level. The function of this protein is not known.
Product Image-89400-382

Respirator Cartridges and Filters, Honeywell Safety

Supplier: Honeywell Safety Products
Description: For use with North Safety Products air purifying dual cartridge respirators (see 56222-944 series).

Image Unavailable-CAAAJ61721-AD

EGTA (ethylene glycol bis(2-aminoethyl ether)-N,N,N',N'-tetraacetic acid) 0.5 M in aqueous solution, autoclaved pH 8.0

Catalog Number: (CAAAJ61721-AD)
Supplier: Thermo Scientific Chemicals
Description: Liquid

Certificates


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