2-Hydroxy-5-nitronicotinic+acid
Supplier:
BeanTown Chemical
Description:
CAS: 1314-35-8; EC No: 215-231-4; MDL No: MFCD00011466; RTECS: YO7760000
Powder; Linear Formula: WO3; MW: 231.85
Melting Point: 1472°; Boiling Point: 1837°
Density (g/mL): 7.16
Moisture Sensitive
Supplier:
BeanTown Chemical
Description:
CAS: 13520-76-8; EC No: 236-862-1; MDL No: MFCD00054136
UN No: UN3260; Haz Class: 8; Packing Group: II
Powder; Linear Formula: WO2Cl2; MW: 286.75
Air Sensitive, Moisture Sensitive
Catalog Number:
(AA10404-H2)
Catalog Number:
(AA10409-H4)
Catalog Number:
(100201-724)
Supplier:
Strem Chemicals Inc
Description:
CAS #: 7440-33-7. Size: 100cm.
Catalog Number:
(AA10408-H7)
Catalog Number:
(AA10403-BU)
Supplier:
BeanTown Chemical
Description:
CAS: 13283-01-7; EC No: 236-293-9; MDL No: MFCD00011463
UN No: UN3260; Haz Class: 8; Packing Group: II
Crystalline; Linear Formula: WCl6; MW: 396.57
Melting Point: 275°; Boiling Point: 347°
Density (g/mL): 3.52
Moisture Sensitive
Catalog Number:
(AA10407-CQ)
Catalog Number:
(AA44191-H9)
Supplier:
Thermo Scientific Chemicals
Description:
0.05mm (0.002in) dia, 99.95% (metals basis)
Catalog Number:
(10802-404)
Supplier:
Rockland Immunochemical
Description:
Defects in the CISD2 (CDGSH iron sulfur domain 2) gene are a cause of the neurodegenerative disorder Wolfram syndrome 2. CISD2 is a zinc finger protein that localizes to the endoplasmic reticulum and mitochondria and binds an iron/sulfur cluster. CISD2 interacts with Bcl-2 and can be displaced by the BH3-only protein BIK and contributes to the regulation of BIK-initiated autophagy. CISD2 deficiency in mice causes mitochondrial breakdown accompanied by autophagic cell death as well as the development of premature aging phenotype.
Catalog Number:
(BT127710-300X3)
Supplier:
BeanTown Chemical
Description:
CAS: 7440-33-7; EC No: 231-143-9; MDL No: MFCD00011461
Wire Cloth; Molecular Formula: W; MW: 183.84
Melting Point: 3410°; Boiling Point: 5660°
Density (g/mL): 19.3
Catalog Number:
(10751-942)
Supplier:
Prosci
Description:
CISD2 Antibody: Defects in the CISD2 (CDGSH iron sulfur domain 2) gene are a cause of the neurodegenerative disorder Wolfram syndrome 2. CISD2 is a zinc finger protein that localizes to the endoplasmic reticulum and mitochondria and binds an iron/sulfur cluster. CISD2 interacts with Bcl-2 and can be displaced by the BH3-only protein BIK and contributes to the regulation of BIK-initiated autophagy. CISD2 deficiency in mice causes mitochondrial breakdown accompanied by autophagic cell death as well as the development of premature aging phenotype.
Supplier:
APOLLO SCIENTIFIC
Description:
Tungsten trioxide 99+%
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