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Catalog Number: (10081-694)
Supplier: Proteintech
Description: Anti-OSTEOCALCIN(Polyclonal) Antibody, Host Species: Rabbit, Cross Reactivity: Human, Immunogen: Fusion Protein, 23-100 amino acid, Format:Antigen Affinity purified, Application: ELISA, IHC, Recommended Storage: - 20 C or lower


Catalog Number: (75811-200)
Supplier: Spectrum Chemicals
Description: FD and C Yellow No. 5 | Non-graded FD and C Yellow No. 5 supplied by Spectrum is indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.


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 Human FGF-acidic is a 16.8 kDa protein consisting of 141 amino acid residues.

Catalog Number: (10072-616)
Supplier: Prosci
Description: BCMA, a member of the TNF receptor superfamily, binds to BAFF and APRIL. BCMA is expressed on mature B-cells and other B-cell lines and plays an important role in B cell development, function and regulation. BCMA also has the capability to activate NF-kappaB and JNK. The human BCMA gene codes for a 184 amino acid type I transmembrane protein, which contains a 54 amino acid extracellular domain, a 23 amino acid transmembrane domain, and a 107 amino acid extracellular domain. Recombinant soluble BCMA is a 50 amino acid polypeptide (5.3 kDa) comprising the TNFR homologous region of the BCMA protein.


Catalog Number: (TCC1713-1G)
Supplier: TCI America
Description: CAS Number: 56683-55-7
MDL Number: MFCD00143276
Molecular Formula: C15H20O7
Molecular Weight: 312.32
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 189

SDS


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: (10490-668)
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: (10110-250)
Supplier: Prosci
Description: ST6GALNAC4 is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. ST6GALNAC4 prefers glycoproteins rather than glycolipids as substrates and shows restricted substrate specificity, utilizing only the trisaccharide sequence Neu5Ac-alpha-2,3-Gal-beta-1,3-GalNAc. In addition, it is involved in the synthesis of ganglioside GD1A from GM1B. ST6GALNAC4 is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. It is a member of glycosyltransferase family 29.The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein prefers glycoproteins rather than glycolipids as substrates and shows restricted substrate specificity, utilizing only the trisaccharide sequence Neu5Ac-alpha-2,3-Gal-beta-1,3-GalNAc. In addition, it is involved in the synthesis of ganglioside GD1A from GM1B. The encoded protein is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. This protein is a member of glycosyltransferase family 29. Transcript variants encoding different isoforms have been found for this gene.


Catalog Number: (89419-394)
Supplier: Prosci
Description: BRSK2 peptide is used for blocking the activity of BRSK2 antibody.


Supplier: Thermo Scientific Chemicals
Description: Potent inhibitor of protein synthesis in bacteria
Supplier: TCI America
Description: CAS Number: 103-23-1
MDL Number: MFCD00009496
Molecular Formula: C22H42O4
Molecular Weight: 370.57
Purity/Analysis Method: >98.0% (GC)
Form: Clear Liquid
Boiling point (°C): 214
Melting point (°C): -70
Flash Point (°C): 205
Specific Gravity (20/20): 0.93
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.


Supplier: MilliporeSigma
Description: Hydrochloric acid 0.1 mol/l (0.1 N), Titripur® Reag. Ph. Eur., Reag. USP volumetric solution, Supelco®
Catalog Number: (10087-468)
Supplier: Proteintech
Description: Anti-GDF8/MYOSTATIN Antibody, Host Species: Rabbit, Cross Reactivity: Human,Mouse,Rat, Immunogen: Fusion Protein, 23-375 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, IHC, Recommended Storage: - 20 C or lower


Catalog Number: (TCI0428-100G)
Supplier: TCI America
Description: CAS Number: 2451-62-9
MDL Number: MFCD00080670
Molecular Formula: C12H15N3O6
Molecular Weight: 297.27
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 108
Flash Point (°C): 170

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.


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