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Image Unavailable-10085-398

Anti-DNAJB11 Rabbit Polyclonal Antibody

Catalog Number: (10085-398)
Supplier: Proteintech
Description: Anti-DNAJB11 Antibody, Host Species: Rabbit, Cross Reactivity: Human,Mouse,Rat, Immunogen: Recombinant Protein, 23-358 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, IHC, IF, Recommended Storage: - 20 C or lower
Image Unavailable-102999-354

Human [Gla17,21,24]-Osteocalcin (1-49) Peptide

Supplier: Anaspec Inc
Description: Osteocalcin (OC) is a 49 amino acid peptide found exclusively in bone tissue and is highly conserved among species. It is a vitamin K- and D-dependent protein produced by osteoblasts, osteocytes and odontoblasts. It is deposited in extracellular bone matrix and is found in the serum. Serum osteocalcin, hydrolysed in the kidney and liver, is considered a specific marker of osteoblast activity and bone formation rate. It may be involved in regulation of osteoblast function, regulation of bone turnover and/or mineralization.
Sequence: YLYQWLGAPVPYPDPL-Gla-PRR-Gla-VC-Gla-LNPDCDELADHIGFQEAYRRFYGPV (Gla=γ-Carboxyglutamic Acid; Disulfide bridge: 23-29)
MW: 5929.5 Da
% Peak area by HPLC: 95
Storage condition: -20° C

Image Unavailable-EM1.00327.5000

Hydrochloric acid in ethanol for microscopy, Sigma-Aldrich®

Supplier: MilliporeSigma
Description: Hydrochloric acid in ethanol is used for the microscopical investigation of mycobacteria in sample material of human origin. It can be applied as decolorizing solution.

Certificates

Image Unavailable-10490-678

Anti-BPGM Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

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.
Image Unavailable-CA1.09057.9010

Hydrochloric acid 1 mol/l (1 N), Titripur® Reag. Ph. Eur., Reag. USP volumetric solution, Supelco®

Supplier: MilliporeSigma
Description: Hydrochloric acid 1 mol/l (1 N), Titripur® Reag. Ph. Eur., Reag. USP volumetric solution, Supelco®

SDS Certificates

Image Unavailable-10072-592

Rat Recombinant FGF Acidic (from E. coli)

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.

Product Image-89419-720

Human RGPD5 Peptide (23 aa in the center)

Catalog Number: (89419-720)
Supplier: Prosci
Description: RGPD5 peptide is used for blocking the activity of RGPD5 antibody.
Product Image-89419-396

Human NogoA Peptide (23 aa near N-terminus)

Catalog Number: (89419-396)
Supplier: Prosci
Description: NogoA peptide is used for blocking the activity of NogoA antibody.
Image Unavailable-10490-670

Anti-BPGM Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10490-670)
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-10490-674

Anti-BPGM Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10490-674)
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-CAAAB22972-22

(-)-Di-p-toluoyl-L-tartaric acid 98%

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

Certificates

Image Unavailable-89520-020

Anti-MANF Rabbit Polyclonal Antibody

Catalog Number: (89520-020)
Supplier: Abgent
Description: Polyclonal antibody, Isotype: Rabbit Ig, Species reactivity: Human, Gene ID: 7873, Target/Specificity: This MANF antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 23-51 amino acids from the N-terminal region of human MANF.
Image Unavailable-89520-138

Anti-MFAP2 Rabbit Polyclonal Antibody

Catalog Number: (89520-138)
Supplier: Abgent
Description: Polyclonal antibody, Isotype: Rabbit Ig, Species reactivity: Human, Gene ID: 4237, Target/Specificity: This MFAP2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 23-52 amino acids from the N-terminal region of human MFAP2.
Product Image-89419-394

Human BRSK2 Peptide (23 aa near C-terminus)

Catalog Number: (89419-394)
Supplier: Prosci
Description: BRSK2 peptide is used for blocking the activity of BRSK2 antibody.
Product Image-10110-250

Anti-ST6GALNAC4 Rabbit Polyclonal Antibody

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.
Product Image-10094-688

Anti-SLAMF7 Rabbit Polyclonal Antibody

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
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