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1,9-Bis(acryloyloxy)nonane
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1,9-Bis(acryloyloxy)nonane
Supplier:
Thermo Scientific Chemicals
Description:
D-Glucosamine sulfate, Purity: 98%, CAS Number: 29031-19-4, Molecular Formula: C6H13NO5.H2SO4, Color: White to off-White, Form: Powder, Synonyms: Chitosamine sulfate, 2-Amino-2-deoxy-D-glucose sulfate, Size: 5G
Supplier:
TCI America
Description:
CAS Number: 18171-19-2
MDL Number: MFCD00053912 Molecular Formula: C6H15ClO2Si Molecular Weight: 182.72 Purity/Analysis Method: >95.0% (GC) Form: Clear Liquid Boiling point (°C): 185 Flash Point (°C): 49 Specific Gravity (20/20): 1.03
Catalog Number:
(470310-686)
Supplier:
Wards
Description:
This simple distillation apparatus is made up of boroscilicate glass.
Supplier:
ACROBIOSYSTEMS INC MS
Description:
SARS-CoV-2 (COVID-19) S1 protein, Fc Tag, ACROBiosystems
Catalog Number:
(76710-680)
Supplier:
AFG BIOSCIENCE LLC
Description:
Human A Disintegrin and metalloProteinase with Thrombospondin Motifs 19 (ADAMTS19) ELISA Kit
Catalog Number:
(89362-654)
Supplier:
Genetex
Description:
Mouse monoclonal [BA-17] to Cytokeratin 19
Catalog Number:
(10663-348)
Supplier:
Bioss
Description:
PLEKHJ1 is a 149 amino acid phosphoprotein that contains one PH (pleckstrin homology) domain and is expressed in testis and liver. The gene that encodes PLEKHJ1 maps to human chromosome 19, which consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 contains the greatest gene density of the human chromosomes and is the genetic home for a number of immunoglobulin superfamily members, including killer cell and leukocyte Ig-like receptors, ICAMs, the CEACAM and PSG families, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes are also linked to chromosome 19.
Catalog Number:
(76110-924)
Supplier:
Bioss
Description:
C19orf21 is a 679 amino acid protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
Catalog Number:
(BT212245-50G)
Catalog Number:
(10480-966)
Supplier:
Bioss
Description:
Dpy-19 (dumpy-19), is a 683 amino acid C. elegans protein that is required to orient the neuroblasts QL and QR correctly on the anterior/posterior axis. Dpy-19 is expressed highly in dorsal hyp7 cells, ventral P cells and lateral V cells, and dorsal and ventral body muscle cells. DPY19L1 (Dpy-19-like protein 1), also known as KIAA0877, is a 675 amino acid multi-pass membrane protein that belongs to the Dpy-19 family. DPY19L1 is expressed as two isoforms produced by alternative splicing and is encoded by a gene mapping to human chromosome 7, which encodes over 1,000 genes and makes up about 5% of the human genome. Diseases associated with chromosome 7 include Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
Supplier:
AMBEED, INC
Description:
6-Methoxy-3,4-dihydronaphthalen-1(2H)-one, Purity: 98%, CAS Number: 1078-19-9, Appearance: Form: Crystal - Powder / Colour: White - Greyish reddish yellow - Yellow, Storage: Sealed in dry, Room Temperature, Size: 10G
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
4-Heptanone 98%
Catalog Number:
(77243-352)
Supplier:
AMBEED, INC
Description:
Oxepan-4-one, Purity: 96%, CAS Number: 62643-19-0, Appearance: Liquid, Storage: Sealed in dry, 2-8 C, Size: 1g
Catalog Number:
(10068-596)
Supplier:
Prosci
Description:
Involved in the organization of myofibers. Together with KRT8, helps to link the contractile apparatus to dystrophin at the costameres of striated muscle.
Catalog Number:
(ABCA_AB212566-100U)
Supplier:
ABCAM INC.
Description:
Anti-Cytokeratin 19 Mouse Monoclonal Antibody [clone: A53-B/A2.26]
Supplier:
TCI America
Description:
CAS Number: 59277-89-3
Molecular Formula: C8H11N5O3 Molecular Weight: 225.21 Purity/Analysis Method: >98.0% (HPLC) Form: Crystal Melting point (°C): 262
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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.
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