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Catalog Number: (TCN0303-100MG)
Supplier: TCI America
Description: CAS Number: 327-57-1
MDL Number: MFCD00064423
Molecular Formula: C6H13NO2
Molecular Weight: 131.18
Purity/Analysis Method: >99.0% (T)
Form: Crystal
Specific rotation [a]20/D: 23 deg (C=5, 5mol/L HCl)

Catalog Number: (75794-312)
Supplier: Prosci
Description: Tryptophan 2,3-dioxygenase (TDO) is a heme-containing dioxygenase catalyzing the addition of molecular oxygen across the 2,3-double bond of the indole ring of tryptophan to form N-formylkynurenine (NFK). In Anopheles gambiae, TDO is the only enzyme able to catalyze the first and rate-limiting step in L-Trp catabolism through the kynurenine pathway. Tryptophan is an essential amino acid for protein synthesis and also the precursor for production of a number of neurotransmitters, such as serotonin and melatonin; in mosquitoes, the kynurenine pathway is essential for eye pigmentation. Conceivably, the tryptophan-using pathways should be regulated in a coordinated manner in mosquitoes as well as in other species and TDO activation/inactivation processes could play an essential role in these phenomena.


Catalog Number: (10094-688)
Supplier: Proteintech
Description: Anti-SLAMF7 Antibody, Host Species: Rabbit, Cross Reactivity: Human, Immunogen: Recombinant Protein, 23-227 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, Recommended Storage: - 20 C or lower


Catalog Number: (TCT2594-25G)
Supplier: TCI America
Description: CAS Number: 55525-27-4
Molecular Formula: C11H16O8
Molecular Weight: 276.24
Purity/Analysis Method: >98.0% (GC)
Form: Clear Liquid
Color: Very Pale Yellow
Boiling point (°C): 150
Specific Gravity (20/20): 1.24

Supplier: TCI America
Description: CAS Number: 72657-23-9
MDL Number: MFCD00063450
Molecular Formula: C5H10O3
Molecular Weight: 118.13
Purity/Analysis Method: >99.0% (GC)
Form: Clear Liquid
Boiling point (°C): 60
Flash Point (°C): 81
Specific Gravity (20/20): 1.07
Specific rotation [a]20/D: -22.5 deg (neat)
Catalog Number: (75788-872)
Supplier: Prosci
Description: Human Chemokine (C-C Motif) Ligand 23 (CCL23) is a small cytokine belonging to the CC chemokine family. CCL23 is also known as myeloid progenitor inhibitory factor MPIF-1, CK8 and SCYA23. CCL23 cDNA encodes a 120 amino acid residue precursor protein with a putative 21 amino acid residue signal peptide that is cleaved to generate a 99 amino acid residue mature CCL23 (amino acids 22 -120). Additional N-terminal Processing of the 99 amino acid residue variant can generate a 75 amino acid residue peptide (amino acid 46-120) that is significantly more active than the 99 amino acid residue variant. CCL23 binds to CCR1 with high affinity and has chemotactic activity for monocytes, dendritic cells, and osteoclast precursors. CCL23 enhances angiogenesis of endothelial cells, but reduces the proliferation of progenitor cells giving rise to granulocyte and monocyte lineages.


Catalog Number: (TCP1300-025G)
Supplier: TCI America
Description: CAS Number: 91-48-5
MDL Number: MFCD00004252
Molecular Formula: C15H12O2
Molecular Weight: 224.26
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Color: White
Melting point (°C): 175

Catalog Number: (10490-676)
Supplier: Bioss
Description: BPGM (2,3-bisphosphoglycerate mutase) is a 259 amino acid protein that belongs to the phosphoglycerate mutase family and exists as a homodimer that plays a crucial role in the regulation of hemoglobin oxygen. Specifically, BPGM catalyzes the conversion of 3-D-glyceroyl phosphate to 2,3-bisD-glycerate (2,3-BPG), a reaction that is essential for controlling the concentration of 2,3-BPG within the cell. The gene encoding BPGM maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Involvement in disease:Defects in BPGM are the cause of bisphosphoglycerate mutase deficiency (BPGMD) . A disease characterized by hemolytic anemia, splenomegaly, cholelithiasis and cholecystitis.


Catalog Number: (10097-290)
Supplier: Proteintech
Description: Anti-ZIP4 Antibody, Host Species: Rabbit, Cross Reactivity: Human, Immunogen: Fusion Protein, 23-327 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, Recommended Storage: - 20 C or lower


Catalog Number: (10083-008)
Supplier: Proteintech
Description: Anti-APOA4 Antibody, Host Species: Rabbit, Cross Reactivity: Human, Immunogen: Recombinant Protein, 23-396 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, IHC, Recommended Storage: - 20 C or lower


Catalog Number: (10094-594)
Supplier: Proteintech
Description: ST8SIA2, also named as SIAT8B and STX, belongs to the glycosyltransferase 29 family. ST8SIA2 may transfer sialic acid through alpha-2,8-linkages to the alpha-2,3-linked and alpha-2,6-linked sialic acid of N-linked oligosaccharides of glycoproteins and may be involved in PSA (polysialic acid) expression. The antibody is specific to ST8SIA2.


Catalog Number: (10086-636)
Supplier: Proteintech
Description: Anti-ERLIN2 Antibody, Host Species: Rabbit, Cross Reactivity: Human,Mouse,Rat, Immunogen: Recombinant Protein, 23-206 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, Recommended Storage: - 20 C or lower


Supplier: Peprotech
Description: FGF-acidic is one of 23 known members of the FGF family. Proteins of this family play a central role during prenatal development, postnatal growth and regeneration of a variety of tissues, by promoting cellular proliferation and differentiation. FGF-acidic is a non-glycosylated heparin binding growth factor that is expressed in the brain, kidney, retina, smooth muscle cells, bone matrix, osteoblasts, astrocytes and endothelial cells. FGF-acidic has the ability to signal through all the FGF receptors. Recombinant Murine FGF-acidic is a 15.9 kDa protein consisting of 141 amino acid residues.

Catalog Number: (10490-672)
Supplier: Bioss
Description: BPGM (2,3-bisphosphoglycerate mutase) is a 259 amino acid protein that belongs to the phosphoglycerate mutase family and exists as a homodimer that plays a crucial role in the regulation of hemoglobin oxygen. Specifically, BPGM catalyzes the conversion of 3-D-glyceroyl phosphate to 2,3-bisD-glycerate (2,3-BPG), a reaction that is essential for controlling the concentration of 2,3-BPG within the cell. The gene encoding BPGM maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Involvement in disease:Defects in BPGM are the cause of bisphosphoglycerate mutase deficiency (BPGMD) . A disease characterized by hemolytic anemia, splenomegaly, cholelithiasis and cholecystitis.


Supplier: Akro-Mils
Description: Super-Size AkroBins offer huge storage capacity and the versatility required to make the most of available space.

Supplier: TCI America
Description: CAS Number: 113826-06-5
MDL Number: MFCD00010834
Molecular Formula: C10H12O4S
Molecular Weight: 228.26
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Color: White
Melting point (°C): 48
Flash Point (°C): 202
Specific rotation [a]20/D: -19 deg (C=2.5, CH3CN)

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