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Catalog Number: (TCH0360-025G)
Supplier: TCI America
Description: CAS Number: 19780-85-9
MDL Number: MFCD00047481
Molecular Formula: C10H21NO2
Molecular Weight: 187.28
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 49

SDS


Supplier: MilliporeSigma
Description: Cas Number 111-77-3, Chemical Formula Hoch2Ch2Och2Ch2Och3, For Synthesis
Catalog Number: (CA8.18382.0500)
Supplier: MilliporeSigma
Description: Cas Number 112-59-4 Chemical Formula Ho(Ch2)2O(Ch2)2O(Ch2)5Ch3 For Synthesis

SDS


Supplier: TCI America
Description: N-(2-Hydroxyethyl)maleimide, Purity: >98.0%(HPLC)(N), CAS number: 1585-90-6, Molecular Formula: C6H7NO3, Molecular Weight: 141.13, Synonym: HEMI, Size: 5G

Supplier: TCI America
Description: (stabilized with BHT)
CAS Number: 111-77-3
MDL Number: MFCD00002871
Molecular Formula: C5H12O3
Molecular Weight: 120.15
Purity/Analysis Method: >99.0% (GC)
Form: Clear Liquid
Boiling point (°C): 193
Melting point (°C): -70
Flash Point (°C): 105
Specific Gravity (20/20): 1.02
Catalog Number: (76108-370)
Supplier: Bioss
Description: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is also associated with mutations to chromosome 2.


Catalog Number: (CA611-905-002)
Supplier: Rockland Immunochemical
Description: Secondary Chicken Anti-IgG (H&L) Reacts with Rabbit (Lapine)


Supplier: New England Biolabs (NEB)
Description: An E.coli strain that carries the cloned PspXI gene from Pseudomanas species A1-1 (S.K. Degtyarev).

Supplier: Thermo Scientific Chemicals
Description: Chloroform 99+% stabilized ethanol-free
Supplier: Biotium
Description: DNA topoisomerases are nuclear enzymes that regulate the topological structure of DNA in eukaryotic cells by transiently breaking and rejoining DNA strands. Due to their roles in DNA replication, recombination, and transcription, DNA topoisomerases have been identified as targets of numerous anticancer drugs. Mitochondrial Topo I (DNA topoisomerase I, mitochondrial) is a 601 amino acid protein that primarily acts to relieve DNA strain that may occur during duplication of mitochondrial DNA. As a type IB topoisomerase, mitochondrial Topo I requires a divalent metal, either, calcium or magnesium, as well as an alkaline pH for optimal activity.

CF® dyes are Biotium's next-generation fluorescent dyes. CF®568 is a red fluorescent dye (Ex/Em 562/583 nm) with superior brightness and photostability. It also is compatible with super-resolution imaging by STORM and TIRF.

Supplier: TCI America
Description: CAS Number: 622-26-4
MDL Number: MFCD00006008
Molecular Formula: C7H15NO
Molecular Weight: 129.20
Purity/Analysis Method: >96.0% (GC,T)
Form: Crystal
Color: White
Boiling point (°C): 228
Melting point (°C): 50
Flash Point (°C): 110
Supplier: Biotium
Description: DNA topoisomerases are nuclear enzymes that regulate the topological structure of DNA in eukaryotic cells by transiently breaking and rejoining DNA strands. Due to their roles in DNA replication, recombination, and transcription, DNA topoisomerases have been identified as targets of numerous anticancer drugs. Mitochondrial Topo I (DNA topoisomerase I, mitochondrial) is a 601 amino acid protein that primarily acts to relieve DNA strain that may occur during duplication of mitochondrial DNA. As a type IB topoisomerase, mitochondrial Topo I requires a divalent metal, either, calcium or magnesium, as well as an alkaline pH for optimal activity.

CF® dyes are Biotium's next-generation fluorescent dyes. CF®594 is a deep red fluorescent dye (Ex/Em 593/614 nm). It yields the brightest conjugates among spectrally similar dyes, and has excellent photostability.

Catalog Number: (CA612-1503)
Supplier: Rockland Immunochemical
Description: Secondary Goat Anti-IgG F(c) Reacts with Rat


Catalog Number: (76110-648)
Supplier: Bioss
Description: FIGNL1 is a 674 amino acid protein belonging to the AAA ATPase family. FIGNL1 exists as a hexamer that undergoes alternative splicing to produce two isoforms. FIGNL1 utilizes magnesium as a cofactor and is phosphorylated upon DNA damage, probably by ATM or ATR. FIGNL1 is suggested to regulate osteoblast proliferation and differentiation. FIGNL1 is encoded by a gene located on human chromosome 7, which consists about 158 million bases, encodes over 1000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.


Catalog Number: (CA80054-462)
Supplier: MilliporeSigma
Description: Nitric oxide (NO) donor. Spontaneously decomposes to yield NO and superoxide anion radicals. Also inhibits release of plasminogen activator inhibitor (PAI) from stimulated platelets. CAS: 16142-27-1.FW: 206.7. Purity: >= 98% by TLC. Soluble in DMSO, ethanol and water. 20mg white solid.

Catalog Number: (10487-956)
Supplier: Bioss
Description: FIGNL1 is a 674 amino acid protein belonging to the AAA ATPase family. FIGNL1 exists as a hexamer that undergoes alternative splicing to produce two isoforms. FIGNL1 utilizes magnesium as a cofactor and is phosphorylated upon DNA damage, probably by ATM or ATR. FIGNL1 is suggested to regulate osteoblast proliferation and differentiation. FIGNL1 is encoded by a gene located on human chromosome 7, which consists about 158 milllion bases, encodes over 1000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.


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