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3-(2,5-Dichlorophenoxy)azetidine
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3-(2,5-Dichlorophenoxy)azetidine
Supplier:
AMBEED, INC
Description:
4-Cyanothiazole 97%
Catalog Number:
(76682-016)
Supplier:
AMBEED, INC
Description:
S-Pyridin-2-yl 3-phenylpropanethioate, Purity: 97%, CAS Number: 43125-15-1, Appearance: Liquid or Solid or Semi-solid, Storage: Inert atmosphere, Room Temperature, Size: 1G
Supplier:
AMBEED, INC
Description:
4-(Pyridin-4-yl)butan-1-ol, Purity: 98%, CAS number: 5264-15-3, Appearance: Colorless to Yellow Liquid, Storage: Inert atmosphere, Room Temperature, Size: 1G
Catalog Number:
(10296-032)
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 LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
Supplier:
TCI America
Description:
2-Chloro-3-fluoro-5-methylpyridine, Purity: >98.0%(GC), CAS Number: 34552-15-3, Molecular Formula: C6H5ClFN, Molecular Weight: 145.56, Synonyms: 6-Chloro-5-fluoro-3-picoline, Size: 1G
Catalog Number:
(77179-396)
Supplier:
ANTIBODIES.COM LLC
Description:
Recombinant rabbit monoclonal [KRT15/8312R] antibody to Cytokeratin 15 for IHC-P with samples derived from Human.
Catalog Number:
(76966-712)
Supplier:
ANTIBODIES.COM LLC
Description:
Mouse monoclonal [KRT15/2959] antibody to Cytokeratin 15 for IF, WB and IHC with samples derived from Human.
Supplier:
AMBEED, INC
Description:
6-(2,4-Difluorophenoxy)-2-((1,5-dihydroxypentan-3-yl)amino)-8-methylpyrido[2,3-d]pyrimidin-7(8H)-one, Purity: 98+%, CAS Number: 449811-01-2, Appearance: White to Yellow Solid, Storage: Keep in dark place, Inert atmosphere, 2-8 C, Size: 5mg
Catalog Number:
(100199-408)
Supplier:
Strem Chemicals Inc
Description:
catASium
Supplier:
AMBEED, INC
Description:
trans-3-Aminocyclopentanecarboxylic acid hydrochloride, Purity: 97%, CAS Number: 1392803-15-4, Appearance: White to Yellow Solid, Storage: Inert atmosphere, Room Temperature, Size: 100mg
Catalog Number:
(10663-382)
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:
(10296-030)
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 LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
Catalog Number:
(77179-682)
Supplier:
ANTIBODIES.COM LLC
Description:
Recombinant rabbit monoclonal [PIP/9076R] antibody to GCDFP 15 for IHC-P with samples derived from Human.
Catalog Number:
(87003-974)
Supplier:
Hemocue
Description:
Centrifuge, Benchtop, Rotor for 1.5–10mL Tubes, 8-Place
Catalog Number:
(TS41624-0010)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Nonylphenol (mixture of isomers) 99%
Supplier:
AMBEED, INC
Description:
1-(2-Amino-4-fluorophenyl)ethanone 95%
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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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