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You Searched For: N-Formylglycine


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N-Formylglycine 98% (by NMR)

Supplier: Ambeed
Description: N-Formylglycine 98% (by NMR)

Image Unavailable-77668-974

N-Formylglycine ethyl ester ≥98%

Supplier: Ambeed
Description: N-Formylglycine ethyl ester ≥98%

New Product

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N-Formylglycine 98%

Supplier: Thermo Scientific Chemicals
Description: 5g CAS: 2491-15-8, MDL: MFCD00037360

SDS Certificates

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N-Formylglycine ≥98.0% (by titrimetric analysis)

Supplier: TCI America
Description: CAS Number: 2491-15-8
MDL Number: MFCD00037360
Molecular Formula: C3H5NO3
Molecular Weight: 103.08
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 147

SDS Certificates

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N-Formylglycine ethyl ester ≥98.0%

Supplier: TCI America
Description: CAS Number: 3154-51-6
MDL Number: MFCD00014125
Molecular Formula: C5H9NO3
Molecular Weight: 131.13
Purity/Analysis Method: >98.0% (GC)
Form: Clear Liquid
Specific Gravity (20/20): 1.15

Certificates

Image Unavailable-75789-582

Human Recombinant SUMF1 (from Cells)

Catalog Number: (75789-582)
Supplier: Prosci
Description: Human Sulfatase Modifying Factor 1 (SUMF1) is a 42kDa protein. SUMF1 is a Ca2+-binging member of the sulfatase-modifying factor family. SUMF1 is a soluble ER lumenal glycoprotein, it converts inactive sulfatases into an active form by transforming a catalytic site cysteine into a formylglycine residue. In the ER, SUMF1 can exist as either a monomer, or a disulfide-linked homodimer or a heterodimer with SUMF2. Three splice isoforms are known.
Image Unavailable-10283-430

Anti-SUMF1 Rabbit Polyclonal Antibody

Catalog Number: (10283-430)
Supplier: Bioss
Description: SUMF1 is a 374 amino acid alternatively spliced protein that localizes to the lumen of the endoplasmic reticulum and belongs to the sulfatase-modifying factor family. Expressed ubiquitously with highest expression in liver, kidney and pancreas, SUMF1 exists as either a monomer, a homodimer or a heterodimer (with SUMF2) and functions to oxidize sulfatase cysteine residues to an active FGIy residue, thereby playing an important role in sulfatase activity. Defects in the gene encoding SUMF1 are the cause of multiple sulfatase deficiency (MSD), a heterogeneous disorder characterized by metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata, hydrocephalus, ichthyosis, neurologic deterioration and developmental delay.
Image Unavailable-10279-334

Anti-SUMF1 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10279-334)
Supplier: Bioss
Description: SUMF1 is a 374 amino acid alternatively spliced protein that localizes to the lumen of the endoplasmic reticulum and belongs to the sulfatase-modifying factor family. Expressed ubiquitously with highest expression in liver, kidney and pancreas, SUMF1 exists as either a monomer, a homodimer or a heterodimer (with SUMF2) and functions to oxidize sulfatase cysteine residues to an active FGIy residue, thereby playing an important role in sulfatase activity. Defects in the gene encoding SUMF1 are the cause of multiple sulfatase deficiency (MSD), a heterogeneous disorder characterized by metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata, hydrocephalus, ichthyosis, neurologic deterioration and developmental delay.
Image Unavailable-10279-332

Anti-SUMF1 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10279-332)
Supplier: Bioss
Description: SUMF1 is a 374 amino acid alternatively spliced protein that localizes to the lumen of the endoplasmic reticulum and belongs to the sulfatase-modifying factor family. Expressed ubiquitously with highest expression in liver, kidney and pancreas, SUMF1 exists as either a monomer, a homodimer or a heterodimer (with SUMF2) and functions to oxidize sulfatase cysteine residues to an active FGIy residue, thereby playing an important role in sulfatase activity. Defects in the gene encoding SUMF1 are the cause of multiple sulfatase deficiency (MSD), a heterogeneous disorder characterized by metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata, hydrocephalus, ichthyosis, neurologic deterioration and developmental delay.
Image Unavailable-10279-338

Anti-SUMF1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10279-338)
Supplier: Bioss
Description: SUMF1 is a 374 amino acid alternatively spliced protein that localizes to the lumen of the endoplasmic reticulum and belongs to the sulfatase-modifying factor family. Expressed ubiquitously with highest expression in liver, kidney and pancreas, SUMF1 exists as either a monomer, a homodimer or a heterodimer (with SUMF2) and functions to oxidize sulfatase cysteine residues to an active FGIy residue, thereby playing an important role in sulfatase activity. Defects in the gene encoding SUMF1 are the cause of multiple sulfatase deficiency (MSD), a heterogeneous disorder characterized by metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata, hydrocephalus, ichthyosis, neurologic deterioration and developmental delay.
Image Unavailable-10279-336

Anti-SUMF1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10279-336)
Supplier: Bioss
Description: SUMF1 is a 374 amino acid alternatively spliced protein that localizes to the lumen of the endoplasmic reticulum and belongs to the sulfatase-modifying factor family. Expressed ubiquitously with highest expression in liver, kidney and pancreas, SUMF1 exists as either a monomer, a homodimer or a heterodimer (with SUMF2) and functions to oxidize sulfatase cysteine residues to an active FGIy residue, thereby playing an important role in sulfatase activity. Defects in the gene encoding SUMF1 are the cause of multiple sulfatase deficiency (MSD), a heterogeneous disorder characterized by metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata, hydrocephalus, ichthyosis, neurologic deterioration and developmental delay.
Image Unavailable-10279-330

Anti-SUMF1 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10279-330)
Supplier: Bioss
Description: SUMF1 is a 374 amino acid alternatively spliced protein that localizes to the lumen of the endoplasmic reticulum and belongs to the sulfatase-modifying factor family. Expressed ubiquitously with highest expression in liver, kidney and pancreas, SUMF1 exists as either a monomer, a homodimer or a heterodimer (with SUMF2) and functions to oxidize sulfatase cysteine residues to an active FGIy residue, thereby playing an important role in sulfatase activity. Defects in the gene encoding SUMF1 are the cause of multiple sulfatase deficiency (MSD), a heterogeneous disorder characterized by metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata, hydrocephalus, ichthyosis, neurologic deterioration and developmental delay.
Image Unavailable-76753-062

Anti-SUMF2 Rabbit Polyclonal Antibody

Catalog Number: (76753-062)
Supplier: Prosci
Description: Anti-SUMF2 Rabbit Polyclonal Antibody
Product Image-77516-074

Human SUMF1 (Sulfatase Modifying Factor 1) ELISA Kit

Catalog Number: (77516-074)
Supplier: AFG Bioscience
Description: Human SUMF1 (Sulfatase Modifying Factor 1) ELISA Kit
Product Image-77063-948

Anti-SUMF1 Goat Polyclonal Antibody

Catalog Number: (77063-948)
Supplier: ANTIBODIES.COM LLC
Description: Goat polyclonal antibody to SUMF1 for ELISA and WB with samples derived from Human and Mouse.
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Human Recombinant Sulfatase-Modifying Factor 1

Supplier: Bon Opus Biosciences
Description: Bon Opus Biosciences offers quality recombinant proteins products covering a broad collection of cytokines, enzymes, diagnostic and detection reagents, and other protein-related products

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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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