You Searched For: 6-Methylflavone

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: 10072-592

Supplier: Prosci

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Description: Cell permeable non-tubulin-interacting mitosis inhibitor. Blocks mitosis (IC50=14µM) by binding to the mitotic kinesin Eg5.

Catalog Number: 89158-918

Supplier: Enzo Life Sciences

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Description: This peptide is Histone H3 amino acid residues 21 to 43. It is monomethylated at lysine 23 with a C-terminal G linker followed by a biotinylated lysine. Provided at >95% peptide purity, this peptide was dissolved in distilled water at 1 mg/ml and re-lyophilized to powder form.
Sequence:AT-K(Me1)-AARKSAPSTGGVKKPHRYRPG-GK(Biotin)-NH2
MW:2946.5 Da
% peak area by HPLC:95
Storage condition:-20° C

Catalog Number: 103008-302

Supplier: Anaspec Inc

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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.

Catalog Number: 10156-132

Supplier: Proteintech

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Description: 7-Azaindole-5-boronic acid pinacol ester 97%

Catalog Number: CAAAAH50044-MD

Supplier: Thermo Scientific Chemicals

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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: 10081-694

Supplier: Proteintech

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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: 10490-678

Supplier: Bioss

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Description: Ultrapure grade, Causes severe skin burns and eye damage, Synonym Hydrogen chloride solution.

Catalog Number: CA1.01514.0250

Supplier: MilliporeSigma

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

Catalog Number: TCG0095-025G

Supplier: TCI America

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Description: (+)-Di-p-toluoyl-D-tartaric acid 98%

Catalog Number: CAAAAL13223-14

Supplier: Thermo Scientific Chemicals

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Description: Anti-TRBV5-4 Antibody, Host Species: Rabbit, Cross Reactivity: Human, Immunogen: Recombinant Protein, 23-276 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, Recommended Storage: - 20 C or lower

Catalog Number: 10096-302

Supplier: Proteintech

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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: 76110-740

Supplier: Bioss

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Description: Hydrochloric acid fuming, Purity:37%, Synonyms:Hydrogen chloride solution, Application:for analysis max. 0.001 ppm Hg EMSURE

Catalog Number: CA1.13386.2500

Supplier: MilliporeSigma

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Description: CAS Number: 1149-23-1
MDL Number: MFCD00005951
Molecular Formula: C13H19NO4
Molecular Weight: 253.30
Purity/Analysis Method: >98.0% (HPLC,N)
Form: Crystal
Melting point (°C): 183
Lambda max.: 374 nm (EtOH)

Catalog Number: TCD3775-1G

Supplier: TCI America

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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: 10495-590

Supplier: Bioss

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Description: Anti-CADM4 Antibody, Host Species: Rabbit, Cross Reactivity: Human,Mouse,Rat, Immunogen: Fusion Protein, 23-321 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, Recommended Storage: - 20 C or lower

Catalog Number: 10083-962

Supplier: Proteintech

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