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1,3,5-Tri(1-naphthyl)benzene
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1,3,5-Tri(1-naphthyl)benzene
Supplier:
AMBEED, INC
Description:
1-Bromo-3-fluoro-5-iodobenzene 98%
Catalog Number:
(10436-180)
Supplier:
Bioss
Description:
C10orf28 is a 792 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding C10orf28 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Supplier:
Showa
Description:
Forged with fluoroelastomer rubber, SHOWA 893 gloves provide superior resistance to highly corrosive acids. They are designed for handling aliphatic and aromatic hydrocarbons, such as benzene, toulene, and xylene.
Catalog Number:
(76120-302)
Supplier:
Bioss
Description:
CWF19L1 is a 538 amino acid protein belonging to the CWF19 family and exists as three alternatively spliced isoforms. CWF19L1 is encoded by a gene located on human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman's syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number:
(10479-412)
Supplier:
Bioss
Description:
FAM13C1, also known as FAM13C, is a 585 amino acid protein that belongs to the FAM13 family. Existing as three alternatively spliced isoforms, the gene encoding FAM13C1 maps to human chromosome 10, which contains over 800 genes, 135 million nucleotides and makes up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.
Supplier:
AMBEED, INC
Description:
4-tert-Butylbenzonitrile 98%
Supplier:
TCI America
Description:
1,3-Benzenedithiol, Purity: >95.0%(GC), Cas number: 626-04-0, Molecular Formula: C6H6S2, Molecular Weight: 142.23, Appearance: White - Almost white solid crystal lump, Synonyms: 1,3-Dimercaptobenzene, Dithioresorcinol, Size: 1G
Supplier:
AMBEED, INC
Description:
Dicyclohexyl(2,4,6-triisopropylphenyl)phosphine, Purity: 97%, CAS number: 303111-96-8, Appearance: Form: Crystal - Powder / Colour: White - Almost white, Storage: Inert atmosphere, Room Temperature, Size: 1G
Supplier:
TCI America
Description:
CAS Number: 3466-32-8
MDL Number: MFCD00025065 Molecular Formula: C7H7BrO2S Molecular Weight: 235.10 Purity/Analysis Method: >98.0% (GC) Form: Crystal Melting point (°C): 104
Supplier:
PeproTech, Inc.
Description:
Human sDLL-4 comprises the extracellular signaling domain of DLL, a member of a structurally-related family of single-pass type I trans-membrane proteins that serve as ligands for Notch receptors. DLL-4 functions to specifically activate the Notch-1 and Notch-4 receptors. The Notch signaling pathway regulates endothelial cell differentiation, proliferation and apoptosis, and is essential for the development, maintenance and remodeling of the vascular system. Targeted deletion of the DLL-4 gene in mice resulted in severe vascular defects and death before birth. Up-regulation of DLL-4 expression has been implicated in the vascular development of certain tumors. The human DLL-4 gene consists of a 503 amino acid extracellular domain with one DSL domain, eight EGF-like repeats, a 21 a.a. transmembrane domain, and a 135 a.a. cytoplasmic domain. Recombinant Human sDLL-4 is a 54.3 kDa glycoprotein containing 498 amino acid residues.
Catalog Number:
(77310-194)
Supplier:
AMBEED, INC
Description:
1,2-Dibromo-4,5-difluorobenzene 98%
Supplier:
ACROBIOSYSTEMS INC MS
Description:
Biotinylated Cynomolgus CD3E&CD3D Heterodimer Protein, His,Avitag™&Tag Free (MALS verified), ACROBiosystems
Catalog Number:
(10162-702)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to Histone H3K36me3 (trimethy Lys36)
Catalog Number:
(10162-724)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to Histone H4K20me3 (trimethyl Lys20)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
1-Bromo-2,4-difluorobenzene 98+%
Supplier:
AMBEED, INC
Description:
1,4-Dibromo-2-nitrobenzene 98%
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 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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