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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:
3,5-Bis(trifluoromethyl)benzenesulfonyl chloride 98%
Supplier:
TCI America
Description:
Carbonylhydridotris(triphenylphosphine)iridium(I), CAS: 17250-25-8, Molecular Formula: C55H46IrOP3, Weight: 1008.11, Synonym: Carbonyltris(triphenylphosphine)iridium(I) Hydride, Tris(triphenylphosphine)iridium(I) Carbonyl Hydride, Size: 200MG
Supplier:
BeanTown Chemical
Description:
CAS: 5419-55-6; EC No: 226-529-9; MDL No: MFCD00008872; RTECS: ED5950000
UN No: UN2616; Haz Class: 3; Packing Group: II
Liquid; Linear Formula: [(CH3)2CHO]3B; Molecular Formula: C9H21BO3; MW: 188.08
Melting Point: -59°; Boiling Point: 139-141°; Flash point: 17°C (63°F)
Density (g/mL): 0.815; Refractive Index: 1.376
Moisture Sensitive
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
2,6-Diisopropylaniline 90+%
Catalog Number:
(76120-738)
Supplier:
Bioss
Description:
C10orf88 is a 445 amino acid protein encoded by a gene that maps to human chromosome 10q26.13. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1200 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:
(102535-676)
Supplier:
Matrix Scientific
Description:
MF=C8H9BRO2S MW=249.13 CAS=53606-06-7 MDL=MFCD00185849 5G
Supplier:
AOB CHEM USA
Description:
2-Chloro-4-(4-morpholinylcarbonyl)benzeneboronic acid ≥97%
Catalog Number:
(76118-184)
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.
Catalog Number:
(103008-034)
Supplier:
Anaspec Inc
Description:
This peptide is Histone H3 amino acid residues 23 to 34 tri-methylated at Lys-27.
Sequence:KAAR-K(Me3)-SAPATGG MW:1156.3 Da % peak area by HPLC:95 Storage condition:-20° C
Catalog Number:
(76120-184)
Supplier:
Bioss
Description:
C10orf140, also known as DLN-1, is an 827 amino acid protein that belongs to the DACH/dachshund family. C10orf140 contains a poly-Alanine region that is highly polymorphic. The gene encoding C10orf140 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 1200 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:
(10479-410)
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:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
4-Chloro-3-(trifluoromethyl)phenyl isocyanate 98%
Catalog Number:
(ABCA_AB213677-100U)
Supplier:
ABCAM INC.
Description:
Anti-Histone H3.3 (methyl K56 + phospho S10 + tri methyl K9) Rabbit Polyclonal Antibody
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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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