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Image Unavailable-89518-482

Anti-MXD1 Rabbit Polyclonal Antibody

Catalog Number: (89518-482)
Supplier: Abgent
Description: Polyclonal antibody, Isotype: Rabbit Ig, Species Reactivity: Human , Gene ID: 4084 , Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 23-50 amino acids from the N-terminal region of human MXD1
Image Unavailable-CA1.00326.1000

Hydrochloric acid 0.1000 M in 2-propanol, Titripur® DIN 51558-1, Supelco®

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.

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Product Image-RCRABH0022.5D1

Hydrochloric acid 37% for trace metal analysis

Catalog Number: (RCRABH0022.5D1)
Supplier: Ricca Chemical
Description: Hydrochloric Acid, 37%, Trace Metals Grade, 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: 2.50L Glass sc

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Product Image-CAPI24308

Hydrochloric acid solution 6N, Sequencing grade, Pierce™

Catalog Number: (CAPI24308)
Supplier: Thermo Scientific
Description: Pierce™ Hydrochloric acid solution, sequencing grade, is purified and packaged to ensure a ninhydrin-negative blank on hydrolysis

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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-89521-266

Anti-BGLAP Rabbit Polyclonal Antibody

Catalog Number: (89521-266)
Supplier: Abgent
Description: polyclonal antibody, Isotype: Rabbit Ig , Species reactivity: Human, Gene ID: 632, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 23-52 amino acids from the Central region of human BGLAP
Image Unavailable-89518-188

Anti-GGT6 Rabbit Polyclonal Antibody

Catalog Number: (89518-188)
Supplier: Abgent
Description: Polyclonal antibody, Isotype: Rabbit Ig, Species Reactivity: Human , Gene ID: 124975 , Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 23-49 amino acids from the N-terminal region of human GGT6
Product Image-CAJT4813-2

MES sodium salt ≥85.0% for biopharmaceutical production, purified, J.T.Baker®

Supplier: AVANTOR PERFORMANCE MATERIAL LLC
Description: Suitable for use in biopharmaceutical manufacturing applications.

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Image Unavailable-75794-312

Recombinant TDO Anopheles gambiae (from E. coli)

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.
Image Unavailable-10781-714

Human Recombinant FGF-acidic (from E. coli)

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.

Image Unavailable-CAAAAH50044-MD

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

Supplier: Thermo Scientific Chemicals
Description: 7-Azaindole-5-boronic acid pinacol ester 97%

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Image Unavailable-10490-668

Anti-BPGM Rabbit Polyclonal Antibody (Cy3®)

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.
Image Unavailable-75788-872

Human Recombinant CCL23 (from E. coli)

Catalog Number: (75788-872)
Supplier: Prosci
Description: Human Chemokine (C-C Motif) Ligand 23 (CCL23) is a small cytokine belonging to the CC chemokine family. CCL23 is also known as myeloid progenitor inhibitory factor MPIF-1, CK8 and SCYA23. CCL23 cDNA encodes a 120 amino acid residue precursor protein with a putative 21 amino acid residue signal peptide that is cleaved to generate a 99 amino acid residue mature CCL23 (amino acids 22 -120). Additional N-terminal Processing of the 99 amino acid residue variant can generate a 75 amino acid residue peptide (amino acid 46-120) that is significantly more active than the 99 amino acid residue variant. CCL23 binds to CCR1 with high affinity and has chemotactic activity for monocytes, dendritic cells, and osteoclast precursors. CCL23 enhances angiogenesis of endothelial cells, but reduces the proliferation of progenitor cells giving rise to granulocyte and monocyte lineages.
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-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-10097-290

Anti-ZIP4 Rabbit Polyclonal Antibody

Catalog Number: (10097-290)
Supplier: Proteintech
Description: Anti-ZIP4 Antibody, Host Species: Rabbit, Cross Reactivity: Human, Immunogen: Fusion Protein, 23-327 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, Recommended Storage: - 20 C or lower
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