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You Searched For: (S)-2,3-Diaminopropanoic+acid+hydrochloride


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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.
Image Unavailable-10072-616

Human Recombinant BCMA (from E. coli)

Catalog Number: (10072-616)
Supplier: Prosci
Description: BCMA, a member of the TNF receptor superfamily, binds to BAFF and APRIL. BCMA is expressed on mature B-cells and other B-cell lines and plays an important role in B cell development, function and regulation. BCMA also has the capability to activate NF-kappaB and JNK. The human BCMA gene codes for a 184 amino acid type I transmembrane protein, which contains a 54 amino acid extracellular domain, a 23 amino acid transmembrane domain, and a 107 amino acid extracellular domain. Recombinant soluble BCMA is a 50 amino acid polypeptide (5.3 kDa) comprising the TNFR homologous region of the BCMA protein.
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-TCC1713-1G

4'-Carboxybenzo-15-crown-5 (4'-carboxybenzo-1,4,7,10,13-pentaoxacyclopentadecane) ≥98.0% (by GC, titration analysis)

Catalog Number: (TCC1713-1G)
Supplier: TCI America
Description: CAS Number: 56683-55-7
MDL Number: MFCD00143276
Molecular Formula: C15H20O7
Molecular Weight: 312.32
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 189

SDS


Image Unavailable-TCP1300-025G

α-Phenylcinnamic acid ≥98.0% (by titrimetric analysis)

Catalog Number: (TCP1300-025G)
Supplier: TCI America
Description: CAS Number: 91-48-5
MDL Number: MFCD00004252
Molecular Formula: C15H12O2
Molecular Weight: 224.26
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Color: White
Melting point (°C): 175

SDS Certificates


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
Image Unavailable-CAAAJ63874-06

Apramycin sulfate 96%

Supplier: Thermo Scientific Chemicals
Description: Potent inhibitor of protein synthesis in bacteria

Certificates

Image Unavailable-10389-574

Anti-CYP24A1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10389-574)
Supplier: Bioss
Description: Has a role in maintaining calcium homeostasis. Catalyzes the NADPH-dependent 24-hydroxylation of calcidiol (25-hydroxyvitamin D(3)) and calcitriol (1-alpha,25-dihydroxyvitamin D(3)). The enzyme can perform up to 6 rounds of hydroxylation of calcitriol leading to calcitroic acid. It also shows 23-hydroxylating activity leading to 1-alpha,25-dihydroxyvitamin D(3)-26,23-lactone as end product.
Image Unavailable-10389-568

Anti-CYP24A1 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10389-568)
Supplier: Bioss
Description: Has a role in maintaining calcium homeostasis. Catalyzes the NADPH-dependent 24-hydroxylation of calcidiol (25-hydroxyvitamin D(3)) and calcitriol (1-alpha,25-dihydroxyvitamin D(3)). The enzyme can perform up to 6 rounds of hydroxylation of calcitriol leading to calcitroic acid. It also shows 23-hydroxylating activity leading to 1-alpha,25-dihydroxyvitamin D(3)-26,23-lactone as end product.
Product Image-10083-008

Anti-APOA4 Rabbit Polyclonal Antibody

Catalog Number: (10083-008)
Supplier: Proteintech
Description: Anti-APOA4 Antibody, Host Species: Rabbit, Cross Reactivity: Human, Immunogen: Recombinant Protein, 23-396 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, IHC, Recommended Storage: - 20 C or lower
Image Unavailable-10094-594

Anti-ST8SIA2 Rabbit Polyclonal Antibody

Catalog Number: (10094-594)
Supplier: Proteintech
Description: ST8SIA2, also named as SIAT8B and STX, belongs to the glycosyltransferase 29 family. ST8SIA2 may transfer sialic acid through alpha-2,8-linkages to the alpha-2,3-linked and alpha-2,6-linked sialic acid of N-linked oligosaccharides of glycoproteins and may be involved in PSA (polysialic acid) expression. The antibody is specific to ST8SIA2.
Product Image-10086-636

Anti-ERLIN2 Rabbit Polyclonal Antibody

Catalog Number: (10086-636)
Supplier: Proteintech
Description: Anti-ERLIN2 Antibody, Host Species: Rabbit, Cross Reactivity: Human,Mouse,Rat, Immunogen: Recombinant Protein, 23-206 amino acid, Format:Antigen affinity purification, Application: ELISA, WB, Recommended Storage: - 20 C or lower
Image Unavailable-10774-786

Mouse 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 Murine FGF-acidic is a 15.9 kDa protein consisting of 141 amino acid residues.

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.
Image Unavailable-TCT2594-25G

Tetramethyl-1,1,2,3-propanetetracarboxylate ≥98.0%

Catalog Number: (TCT2594-25G)
Supplier: TCI America
Description: CAS Number: 55525-27-4
Molecular Formula: C11H16O8
Molecular Weight: 276.24
Purity/Analysis Method: >98.0% (GC)
Form: Clear Liquid
Color: Very Pale Yellow
Boiling point (°C): 150
Specific Gravity (20/20): 1.24

SDS Certificates


Image Unavailable-10490-672

Anti-BPGM Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (10490-672)
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.
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