You Searched For: N-Formyl-L-methionine


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Supplier: Ambeed
Description: Glycyl-L-methionine

New Product

Catalog Number: (TCD1034-001G)
Supplier: TCI America
Description: MDL Number: MFCD00070531
Molecular Formula: C11H13N3O6S
Molecular Weight: 496.62
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Specific rotation [a]20/D: -24 deg (C=1, MeOH)

SDS


Catalog Number: (76864-596)
Supplier: ANTIBODIES.COM LLC
Description: Rabbit polyclonal antibody to Methionine Sulfoxid eReductase B for WB and ICC/IF with samples derived from Human, Mouse and Rat.


Catalog Number: (77518-648)
Supplier: AFG Bioscience
Description: Human MSRA (Methionine Sulfoxide Reductase A) ELISA Kit

New Product


Catalog Number: (10108-540)
Supplier: Prosci
Description: MAT1A catalyzes a two-step reaction that involves the transfer of the adenosyl moiety of ATP to methionine to form S-adenosylmethionine and tripolyphosphate, which is subsequently cleaved to PPi and Pi. S-adenosylmethionine is the source of methyl groups for most biological methylations. MAT1A is found as a homotetramer (MAT I) or a homodimer (MAT III) whereas a third form, MAT II (gamma), is encoded by the MAT2A gene. Mutations in its gene are associated with methionine adenosyltransferase deficiency.This gne encodes methionine adenosyltransferase I (alpha isoform), which catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.


Catalog Number: (77528-248)
Supplier: AFG Bioscience
Description: MEK (Methionine-Enkephalin) ELISA Kit

New Product


Catalog Number: (77215-898)
Supplier: ANTIBODIES.COM LLC
Description: Human Methionine Aminopeptidase 2/p67 ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the <i>in vitro</i> quantitative determination of human Methionine Aminopeptidase 2/p67 in serum, plasma, and other biological fluids.


Catalog Number: (10033-746)
Supplier: Enzo Life Sciences
Description: Produced in insect cells. Recombinant, full-length (aa 1-478) methionine aminopeptidase 2 with an N-terminal hemagglutinin (HA) tag (YPYDVPDYA), cloned from human cDNA.


Catalog Number: (220024-294)
Supplier: R&D Systems
Description: The Recombinant Human Methionine Aminopeptidase 1 Protein from R&D Systems is derived from Sf 21 (baculovirus). The Recombinant Human Methionine Aminopeptidase 1 Protein has been validated for the following applications: Enzyme Activity.


Catalog Number: (220024-407)
Supplier: R&D Systems
Description: The Recombinant Human Methionine Aminopeptidase 2 Protein from R&D Systems is derived from Sf 21 (baculovirus). The Recombinant Human Methionine Aminopeptidase 2 Protein has been validated for the following applications: Enzyme Activity.


Catalog Number: (PAL9961)
Supplier: Promega Corporation
Description: Amino Acid Mixture, Complete, is an aqueous solution containing 1mM each of the 20 essential amino acids.

Catalog Number: (MSPP-PAG414GE1)
Supplier: CLOUD-CLONE CORP MS
Description: Polyclonal Antibody to S-Adenosyl Methionine (SAM), derived from OVA conjugated SAM, is reactive with General species.

New Product


Catalog Number: (76085-736)
Supplier: Bioss
Description: S adenosylmethionine synthetase catalyzes the formation of S adenosylmethionine from methionine and ATP. In mammalian tissues, there are three distinct forms of AdoMet synthases designated as alpha, beta, and gamma. Alpha and beta are expressed only in adult liver, while gamma is widely distributed in extrahepatic tissues.


Catalog Number: (10108-538)
Supplier: Prosci
Description: MAT1A catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.This gne encodes methionine adenosyltransferase I (alpha isoform), which catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.


Supplier: Ambeed
Description: Fmoc-Met(O)-OH 95%

Supplier: Ambeed
Description: H-Met-Pna ≥97%, Ambeed.Inc

New Product

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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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