1,2-Cyclohexanedione
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
4-Amino-2-hydroxypyridine 97%
Catalog Number:
(76120-558)
Supplier:
Bioss
Description:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf42 gene product has been provisionally designated C12orf42 pending further characterization.
Catalog Number:
(470343-622)
Supplier:
Wards
Description:
This rack is made of durable polypropylene and securely holds test tubes with diameters of 30, 20, 17 and 12 mm for organized laboratory storage.
Supplier:
Chemglass
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Supplier:
AOB CHEM USA
Description:
1-(Benzyloxy)-4-bromo-2-(tert-butyl)benzene ≥97%
Supplier:
Sklar
Description:
The Mayo Tray holds instruments to be used in a surgical procedure
Supplier:
ABCAM INC.
Description:
Anti-Myelin Basic Protein Rat Monoclonal Antibody [clone: 12]
Supplier:
AGILENT TECHNOLOGIES, INC (CSD)
Description:
These 2 ml crimp top vials and matching crimp caps are engineered to protect against sample loss.
Supplier:
Matrix Scientific
Description:
MF=C6H4Cl2S MW=179.07 Cas=5858-17-3 MDL=MFCD00004840 25G
Catalog Number:
(76120-544)
Supplier:
Bioss
Description:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf4 gene product has been provisionally designated C12orf4 pending further characterization.
Supplier:
AMBEED, INC
Description:
2-Chloro-5-fluoropyrimidin-4-one, Purity: 95%, CAS Number: 155-12-4, Appearance: Form: Crystal - Powder / Colour: White - Slightly pale yellow, Storage: Inert atmosphere, 2-8 deg C, Size: 250mg
Catalog Number:
(101929-898)
Supplier:
Matrix Scientific
Description:
MF=C5H8N4 MW=124.15 Cas=17584-12-2 MDL=MFCD00006460 500Mg
Supplier:
Spectrum Chemicals
Description:
Heptyl 4-Hydroxybenzoate, Purity: 98.0 %, Cas number: 1085-12-7, Molecular formula: C14H20O3, Molecular Weight: 236.31, Color/Appearance: White, Crystals, Powder, Synonyms: Heptylparaben, 4-Hydroxybenzoic Acid Heptyl Ester, Size: 100G
Supplier:
HETTICH INSTRUMENTS
Description:
The Hettich Lab Technology EBA 280 clinical tabletop centrifuge series delivers 90° flat separation for all standard blood, pediatric and urine (collection and analysis) tubes.
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Supplier:
AMBEED, INC
Description:
1,3-Bis(diphenylphosphino)propane 97%
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