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Image Unavailable-10778-554

Human Recombinant IFN-?1 (from E. coli)

Description: IFN λ1, 2, and 3 (also known as IL-29, IL-28A and IL-28B respectively) are distantly related to the IL-10 family and the interferons. All three IFN-lambdas use a distinct receptor system composed of an IFN-λR1 subunit (also called CRF2-12) and IL-10R2 subunit (also called CRF2-14). Signaling through this receptor system induces antiviral defenses similar to, but distinct from, that of type I interferons. Recombinant Human IFN-λ1 is a 19.8 kDa protein containing 178 amino acid residues.
Catalog Number: 10778-554
Supplier: Peprotech
Image Unavailable-RL010-001-B66

Mouse Recombinant Ebi3 (from E. coli)

Description: Epstein-Barr Virus Induced Gene-3 (EBI-3), is a secreted glycoprotein belonging to the hematopoietin receptor family and related to the p40 subunit of IL-12. It was identified by its induced expression in B-lymphocytes in response to Epstein-Barr virus infection. EBI-3 forms heterodimers with p28 to form IL-27 and with p35 to form IL-35. Both IL-27 and IL-35 have anti-inflammatory and regulatory activity. Recombinant Mouse EBI is a non-glycosylated polypeptide chain consisting of 207 amino acids with a molecular weight of 22,900 Da.
Catalog Number: RL010-001-B66
Supplier: Rockland Immunochemical

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Image Unavailable-76118-092

Anti-Acid sphingomyelinase Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Description: Converts sphingomyelin to ceramide. Also has phospholipase C activities toward 1,2-diacylglycerolphosphocholine and 1,2-diacylglycerolphosphoglycerol. Isoform 2 and isoform 3 have lost catalytic activity.Involvement in disease: Defects in SMPD1 are the cause of Niemann-Pick disease type A (NPDA) ; also known as Niemann-Pick disease classical infantile form. It is an early-onset lysosomal storage disorder caused by failure to hydrolyze sphingomyelin to ceramide. It results in the accumulation of sphingomyelin and other metabolically related lipids in reticuloendothelial and other cell types throughout the body, leading to cell death. Niemann-Pick disease type A is a primarily neurodegenerative disorder characterized by onset within the first year of life, mental retardation, digestive disorders, failure to thrive, major hepatosplenomegaly, and severe neurologic symptoms. The severe neurological disorders and pulmonary infections lead to an early death, often around the age of four. Clinical features are variable. A phenotypic continuum exists between type A (basic neurovisceral) and type B (purely visceral) forms of Niemann-Pick disease, and the intermediate types encompass a cluster of variants combining clinical features of both types A and B.
Catalog Number: 76118-092
Supplier: Bioss
Image Unavailable-76117-442

Anti-C12orf23 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Description: C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a number of skeletal deformities, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy.
Catalog Number: 76117-442
Supplier: Bioss
Image Unavailable-TCD0612-5G

3,5-Diiodo-L-tyrosine dihydrate ≥98.0% (by titrimetric analysis)

Description: CAS Number: 18835-59-1
MDL Number: MFCD00016542
Molecular Formula: C9H9I2NO3
Molecular Weight: 432.98
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 213
Specific rotation [a]20/D: 1.2 deg (C=5, 1mol/L HCl)
Catalog Number: TCD0612-5G
Supplier: TCI America
Image Unavailable-10490-010

Anti-TSPAN9 Rabbit Polyclonal Antibody (Cy7®)

Description: The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Catalog Number: 10490-010
Supplier: Bioss
Image Unavailable-10490-004

Anti-TSPAN9 Rabbit Polyclonal Antibody (Cy3®)

Description: The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Catalog Number: 10490-004
Supplier: Bioss
Product Image-89149-064

Catharanthine tartrate (from Catharanthus roseus) ≥90% (dry basis)

Description: Starting material for the synthesis of the antitumor drugs vinblastine and vincristine. It is less active as an inhibitor of tubulin self-assembly into microtubules than the latter two compounds.
Catalog Number: 89149-064
Supplier: Enzo Life Sciences
Image Unavailable-CAAAA12584-0E

Phthalimide 99%

Description: MDL: MFCD00005881 Beilstein: 118522 Slightly soluble in water. Soluble in aqueous alkali hydroxides
Catalog Number: CAAAA12584-0E
Supplier: Thermo Scientific Chemicals

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Product Image-CA97026-246

EDTA 0.716 M, cartridge for digital titrator

Description: EDTA standard solution. Used for the determination of iron by Digital Titrator titration.
Catalog Number: CA97026-246
Supplier: Hach
Image Unavailable-76109-312

Anti-TSPAN9 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Description: The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Catalog Number: 76109-312
Supplier: Bioss
Product Image-10216-950

OTAL Foot Pumps, Bürkle

Description: Delivery tubes made of PP are resistant against weak acids, caustic solutions and detergents.
Delivery tubes made of PVDF are especially for acids and caustic solutions; not for strongly oxidizing acids and caustic solutions.
Delivery tubes made of stainless steel 304 are for solvents and liquids of VbF Hazard Class AIII (not easily flammable).
Battery pump for safe filling of car batteries with acid or distilled water.
Catalog Number: 10216-950
Supplier: BURKLE INC
Image Unavailable-CA700009-854

Ammonium sulfate ≥99%, crystals ACS

Description: Ammonium Sulfate, Crystal, Reagent, ACS is an inorganic salt that is very soluble in water most often used as a soil fertilizer to release minute amounts of acid. It is also used in biochemistry as a precipitant to purify protein, used as a flame retardant.
Catalog Number: CA700009-854
Supplier: Spectrum Chemicals

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Image Unavailable-10458-572

Anti-ZDHHC12 Rabbit Polyclonal Antibody

Description: Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. ZDHHC12 (zinc finger, DHHC domain containing 12), also known as ZNF400, is a 267 amino acid multi-pass membrane protein that contains one DHHC-type zinc finger and is thought to function as a palmitoyltransferase, catalyzing the transformation of palmitoyl-CoA and a cysteine-conjugated protein to a S-palmitoyl protein and free CoA. Three isoforms exist due to alternative splicing events. The gene encoding ZDHHC12 maps to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Chromosome 9 is considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype.
Catalog Number: 10458-572
Supplier: Bioss
Product Image-CA14399-01

EDTA 0.800 M, cartridge for digital titrator

Description: For determination of Calcium and Total Hardness by Digital Titrator titration.
Catalog Number: CA14399-01
Supplier: Hach
Product Image-30620-296

Printed Cylinders, Dynalon

Description: These cylinders feature permanently easy to read blue screened graduations that resist fading and scratching after repeated autoclaving. Meets stringent international quality criteria according to ISO 6706 standards. Tolerances according to DIN 12 680 TT, Class B. Maximum temperature: PP 121°C, PMP 135°C.
Catalog Number: 30620-296
Supplier: Dynalon
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