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Supplier: Prosci
Description: FGF-acidic is one of 23 known members of the FGF family. Proteins of this family play a central role during prenatal development and 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: (10490-678)
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: (10087-582)
Supplier: Proteintech
Description: Anti-GLIPR1L1 Antibody, Host Species: Rabbit, Cross Reactivity: Human, Immunogen: Fusion Protein, 23-233 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, IHC, Recommended Storage: - 20 C or lower


Catalog Number: (10156-132)
Supplier: Proteintech
Description: The Claudin 23 Antibody from Proteintech is a rabbit polyclonal Antibody to a fusion protein of human Claudin 23. This Antibody recognizes human Antigen. The Claudin 23 Antibody has been validated for the following applications: ELISA, IHC, WB analysis.


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: (TCT2231-25G)
Supplier: TCI America
Description: CAS Number: 1323-03-1
Molecular Formula: C17H34O3
Molecular Weight: 286.46
Purity/Analysis Method: >75.0% (GC)
Form: Crystal
Color: White
Freezing point (°C): 23

Supplier: Bachem Americas
Description: See also G-4745, H-3996, the branched substrates H-2416, and L-2070, and the product families 'Glutathione-Related Peptides' and 'Ophthalmic Acid'.

Supplier: Spectrum Chemicals
Description: Sodium Bitartrate, Monohydrate, BiotechGrade, also known as monosodium tartrate, is a sodium acid salt of tartaric acid and used as an acidity regulator as well as a test for ammonium cation. Spectrum offers highly pure reagents suitable for biochemical research and analysis. The critical parameters involved are absence of inhibitors such as traces of heavy metals as well as biochemical function tests for enzymes, coenzymes and enzyme substrates.
Supplier: Thermo Scientific Chemicals
Description: Tartrazine ≥85% (dye content), orange powder
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: (CA1.00326.1000)
Supplier: MilliporeSigma
Description: Synonym Hydrogen chloride solution, acc. to DIN 51558 part 1 c(HCl) = 0.1 mol/l (0,1 N) Titripur gade.

Supplier: TCI America
Description: CAS Number: 27214-00-2
MDL Number: MFCD00042643
Molecular Formula: C3H9O6P
Molecular Weight: 210.13
Purity/Analysis Method: >95.0% (T)
Form: Crystal

SDS

Supplier: Thermo Scientific Chemicals
Description: (-)-Di-p-toluoyl-L-tartaric acid 98%
Catalog Number: (89515-566)
Supplier: Abgent
Description: polyclonal antibody Isotype: Rabbit Ig, Species Reactivity: human, Target/specificity: This PLGLA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 23-48 amino acids from the N-terminal region of human PLGLA.


Catalog Number: (76110-738)
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 1000 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: (10082-464)
Supplier: Proteintech
Description: ACSM2A(Acyl-coenzyme A synthetase ACSM2A, mitochondrial) is also named as ACSM2, MACS2 and belongs to the ATP-dependent AMP-binding enzyme family. It acts as a medium-chain fatty acid : CoA ligase with the caculated molecular weight of 64 kDa and acts on acids from C(4) to C(11) and on the corresponding 3-hydroxy- and 2,3- or 3,4-unsaturated acids.


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