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Sodium bitartrate monohydrate ≥99.5%, BiotechGrade

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.

Certificates

Image Unavailable-76110-738

Anti-BPGM Rabbit Polyclonal Antibody (Alexa Fluor® 680)

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.
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Titanium(IV) isopropoxide 97+%

Supplier: Thermo Scientific Chemicals
Description: Catalyzes the regio selective ring opening of 2,3 epoxy alcohols and acids

Certificates

Image Unavailable-76110-740

Anti-BPGM Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76110-740)
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.
Product Image-10082-464

Anti-ACSM2A Rabbit Polyclonal Antibody

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.
Image Unavailable-10495-590

Anti-BPGM Rabbit Polyclonal Antibody

Catalog Number: (10495-590)
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.
Image Unavailable-CA1.01514.0250

Hydrochloric acid 30%, Ultrapure for trace metal analysis, Supelco®

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

SDS Certificates

Product Image-CA1.09494.0100

Multi Element Standards for ICP, Certipur®, MilliporeSigma

Supplier: MilliporeSigma
Description: Traceable to standard reference material from NIST.

SDS Certificates

Image Unavailable-89158-918

Monastrol ≥98% (by TLC)

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

Image Unavailable-CAAAAL13223-14

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

Supplier: Thermo Scientific Chemicals
Description: (+)-Di-p-toluoyl-D-tartaric acid 98%

Certificates

Image Unavailable-CAHX0607-1

Hydrochloric acid 34 - 37%, OmniTrace® for trace metal analysis, Supelco®

Supplier: MilliporeSigma
Description: For elemental metal analysis via atomic absorption and ICP instruments. Actual Lot Analysis on label. Color-coded label to match acid cap.

SDS Certificates

Image Unavailable-G-2005.1000BA

H-Glu(Tyr-OH)-OH

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'.

Product Image-RCR3780000-1A

Hydrochloric acid 12.0 N

Supplier: Ricca Chemical
Description: Hydrochloric Acid, 12.0 Normal, Cas number: 7647-01-0, 7732-18-5, Molecular Formula: HCl, H2O, Molecular weight: 36.46g/mol, 18.01g/mol, Appearance/Form: Colorless to slightly greenish-yellow liquid, Size: 2500 ml

Certificates

Image Unavailable-10166-206

Anti-ANKRD23 Rabbit Polyclonal Antibody

Catalog Number: (10166-206)
Supplier: Genetex
Description: Rabbit Polyclonal antibody to ANKRD23 (ankyrin repeat domain 23)
Image Unavailable-CA1.13386.2500

Hydrochloric acid fuming 37%, EMSURE® for analysis (max. 0.001 ppm Hg), Supelco®

Catalog Number: (CA1.13386.2500)
Supplier: MilliporeSigma
Description: Hydrochloric acid fuming, Purity:37%, Synonyms:Hydrogen chloride solution, Application:for analysis max. 0.001 ppm Hg EMSURE

SDS Certificates


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Tartrazine ≥85% (dye content), orange powder

Supplier: Thermo Scientific Chemicals
Description: Tartrazine ≥85% (dye content), orange powder

Certificates

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