3-(Hydroxymethyl)-2-methylphenylboronic+acid
Supplier:
PIP
Description:
Tough, sheer PolyTuff polyurethane (1.5 mil) film affords a high degree of tactile sensitivity.
Catalog Number:
(77524-082)
Supplier:
AFG BIOSCIENCE LLC
Description:
Human ARL15 (ADP Ribosylation Factor Like Protein 15) ELISA Kit
Catalog Number:
(100199-408)
Supplier:
Strem Chemicals Inc
Description:
catASium
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: 25mg
Supplier:
AOB CHEM USA
Description:
4-Ethoxy-5-fluoro-2-methylbenzaldehyde ≥97%
Supplier:
AOB CHEM USA
Description:
3-Bromo-2-methoxy-5-methylbenzaldehyde ≥97%
Supplier:
AOB CHEM USA
Description:
4-Fluoro-2-(phenylethynyl)aniline ≥95%
Supplier:
AOB CHEM USA
Description:
2-Bromo-6-(methoxymethyl)pyridine 97%
Supplier:
National Marker
Description:
Unlike other exit signs, easy to install EcoExit™ signs offer the only nonradioactive, zero electrical wiring and virtually no maintenance solution on the market
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Catalog Number:
(77517-864)
Supplier:
AFG BIOSCIENCE LLC
Description:
Human KLF15 (Kruppel Like Factor 15) ELISA Kit
Supplier:
Thermo Scientific Chemicals
Description:
MDL: MFCD00001032
Beilstein Registry No.: 2051549
Supplier:
TCI America
Description:
CAS Number: 4792-15-8
MDL Number: MFCD00002878 Molecular Formula: C10H22O6 Molecular Weight: 238.28 Purity/Analysis Method: >95.0% (GC) Form: Clear Liquid Color: Colorless Boiling point (°C): 184 Flash Point (°C): 113 Specific Gravity (20/20): 1.13
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.
Supplier:
Matrix Scientific
Description:
MF=C8H9CLFN MW=173.62 CAS=685565-15-5 MDL=MFCD09832541 1G
Supplier:
United Scientific Supplies
Description:
Designed for particulate or biological contamination analysis of small volumes using a vacuum filter.
Catalog Number:
(75835-040)
Supplier:
Restek
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