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Disodium+naphthalene-1,5-disulphonate
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Disodium+naphthalene-1,5-disulphonate
Supplier:
AAT BIOQUEST INC
Description:
This compound is the precursor for a variety of AFC enzyme substrates.
Supplier:
Bio-Rad
Description:
Affi-Gel 10 and Affi-Gel 15 gels are activated affinity media that provide spontaneous, rapid, and highly efficient coupling of ligands via primary amines
Catalog Number:
(76285-444)
Supplier:
G-Biosciences
Description:
Magnetic stand is designed for the efficent pull down of magnetic beads in 1.5 and 2 ml micro centrifgue tubes.
Catalog Number:
(10663-394)
Supplier:
Bioss
Description:
GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
Catalog Number:
(77404-822)
Supplier:
APOLLO SCIENTIFIC
Description:
2-(4-Methoxybenzoyl)benzenecarboxylic acid 95%
Supplier:
AMBEED, INC
Description:
5-(4-(2-(5-Ethylpyridin-2-yl)ethoxy)benzyl)thiazolidine-2,4-dione hydrochloride, Purity: 99%, CAS number: 112529-15-4, Appearance: Form: Crystal - Powder / Colour: White - Pale-yellow, Storage: Inert atmosphere, Room Temperature, Size: 25G
Supplier:
AMBEED, INC
Description:
4-(Furan-2-yl)but-3-en-2-one, Purity: 95%, CAS Number: 623-15-4, Appearance: Solid or Semi-solid or liquid or lump, Storage: Keep in dark place, Inert atmosphere, 2-8C, Size: 1G
Supplier:
AOB CHEM USA
Description:
3-Chloro-4-ethoxybenzoic acid ≥97%
Catalog Number:
(101786-526)
Supplier:
Matrix Scientific
Description:
MF=C7H7Fs MW=142.20 Cas=371-15-3 MDL=MFCD00040829 25G
Supplier:
AMBEED, INC
Description:
5-Methoxy-2-tetralone 95%
Catalog Number:
(76821-006)
Supplier:
AMBEED, INC
Description:
4-Chloro-1H-pyrrolo[2,3-c]pyridine, Purity: 95%, CAS Number: 1188313-15-6, Appearance: Pale-yellow to Yellow-brown to Brown Solid, Storage: Sealed in dry, Room Temperature, Size: 250MG
Supplier:
SCAT AMERICAS, INC.
Description:
In order to prevent static discharge with fluids in plastic containers, the contents of the waste receptacles can be secured with ground connection. This allows users to establish an additional safety factor when collecting combustible fluids.
Supplier:
Spectrum Chemicals
Description:
L-Carnitine, Free Base is a quaternary ammonium compound and most commonly used as a nutritional supplement.
Catalog Number:
(76235-324)
Supplier:
Dukal
Description:
Allows care-providers to wash and rinse the hair of a bedridden patient.
Supplier:
Thermo Scientific Chemicals
Description:
(S)-(+)-alpha-Ethylphenylacetic acid. Grade: 99. Melting Point C. Boiling Point C: 270-272*. C10H12O2. 4286-15-1. HARMFUL IRRITANT
Catalog Number:
(10246-086)
Supplier:
Bioss
Description:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM98 gene product has been provisionally designated FAM98 pending further characterization.
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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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The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
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