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You Searched For: ST. GOBAIN - TAUNTON


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Product Image-89150-900

Noc-7 ≥96% (by HPLC)

Description: Nitric oxide (NO) donor.
Catalog Number: 89150-900
Supplier: Enzo Life Sciences
Product Image-89150-904

Noc-12 ≥97% (by HPLC)

Description: Nitric oxide (NO) donor.
Catalog Number: 89150-904
Supplier: Enzo Life Sciences
Product Image-89150-894

Noc-5 ≥90% (by HPLC)

Description: Nitric oxide (NO) donor.
Catalog Number: 89150-894
Supplier: Enzo Life Sciences
Image Unavailable-102988-770

DETA NONOate (NOC-18)

Description: Nitric oxide (NO) donor. The slow release of NO allows the use in experiments investigating the effects of prolonged constant NO delivery to cells and tissues. The half-life time is 20 hours at 37°C and 56 hours at 22-25°C in 0.1M phosphate buffer, pH 7.4. Liberates 2 mol of NO per mol of parent compound. Decomposition of NONOates is nearly instantaneous at pH 5.0.
Catalog Number: 102988-770
Supplier: Adipogen
Image Unavailable-89150-880

DETA NONOate (NOC-18) ≥97% (by 1H-NMR)

Description: Nitric oxide (NO) donor.
Catalog Number: 89150-880
Supplier: Enzo Life Sciences
Product Image-89150-886

MAHMA NONOate ≥98%

Description: Nitric oxide (NO) donor.
Catalog Number: 89150-886
Supplier: Enzo Life Sciences
Product Image-10102-206

Anti-ZNF703 Rabbit Polyclonal Antibody

Description: ZNF703 belongs to the Elbow/Noc family. It contains 1 C2H2-type zinc finger.ZNF703 may function as a transcriptional repressor.
Catalog Number: 10102-206
Supplier: Prosci
Image Unavailable-TCP0872-500G

Polyethylene glycol monolaurate, M.W. n=∼10

Description: CAS Number: 31943-11-0
MDL Number: MFCD00148005
Form: Clear Liquid
Color: Colorless
Flash Point (°C): 250
Specific Gravity (20/20): 1.04
Catalog Number: TCP0872-500G
Supplier: TCI America

SDS Certificates


Image Unavailable-89150-888

PAPA NONOate ≥97%

Description: Nitric oxide (NO) donor.
Catalog Number: 89150-888
Supplier: Enzo Life Sciences
Image Unavailable-10301-492

Anti-ZNF503 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Description: Nolz 1 is a 646 amino acid nuclear protein that is thought to function as a transcriptional repressor and is highly expressed in developing striatum. Additionally, Nolz-1 has been suggested to play a role in neural differentiation. A member of the Elbow/Noc family, Nolz-1 exists as three alternatively spliced isoforms and contains one C2H2-type zinc finger. The gene encoding Nolz-1 maps to human chromosome 10, which makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number: 10301-492
Supplier: Bioss
Image Unavailable-10301-490

Anti-ZNF503 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Description: Nolz 1 is a 646 amino acid nuclear protein that is thought to function as a transcriptional repressor and is highly expressed in developing striatum. Additionally, Nolz-1 has been suggested to play a role in neural differentiation. A member of the Elbow/Noc family, Nolz-1 exists as three alternatively spliced isoforms and contains one C2H2-type zinc finger. The gene encoding Nolz-1 maps to human chromosome 10, which makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number: 10301-490
Supplier: Bioss
Image Unavailable-10301-486

Anti-ZNF503 Rabbit Polyclonal Antibody (Cy5®)

Description: Nolz 1 is a 646 amino acid nuclear protein that is thought to function as a transcriptional repressor and is highly expressed in developing striatum. Additionally, Nolz-1 has been suggested to play a role in neural differentiation. A member of the Elbow/Noc family, Nolz-1 exists as three alternatively spliced isoforms and contains one C2H2-type zinc finger. The gene encoding Nolz-1 maps to human chromosome 10, which makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number: 10301-486
Supplier: Bioss
Image Unavailable-10301-484

Anti-ZNF503 Rabbit Polyclonal Antibody (Cy3®)

Description: Nolz 1 is a 646 amino acid nuclear protein that is thought to function as a transcriptional repressor and is highly expressed in developing striatum. Additionally, Nolz-1 has been suggested to play a role in neural differentiation. A member of the Elbow/Noc family, Nolz-1 exists as three alternatively spliced isoforms and contains one C2H2-type zinc finger. The gene encoding Nolz-1 maps to human chromosome 10, which makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number: 10301-484
Supplier: Bioss
Image Unavailable-10303-232

Anti-ZNF503 Rabbit Polyclonal Antibody

Description: Nolz 1 is a 646 amino acid nuclear protein that is thought to function as a transcriptional repressor and is highly expressed in developing striatum. Additionally, Nolz-1 has been suggested to play a role in neural differentiation. A member of the Elbow/Noc family, Nolz-1 exists as three alternatively spliced isoforms and contains one C2H2-type zinc finger. The gene encoding Nolz-1 maps to human chromosome 10, which makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number: 10303-232
Supplier: Bioss
Image Unavailable-10301-488

Anti-ZNF503 Rabbit Polyclonal Antibody (Cy7®)

Description: Nolz 1 is a 646 amino acid nuclear protein that is thought to function as a transcriptional repressor and is highly expressed in developing striatum. Additionally, Nolz-1 has been suggested to play a role in neural differentiation. A member of the Elbow/Noc family, Nolz-1 exists as three alternatively spliced isoforms and contains one C2H2-type zinc finger. The gene encoding Nolz-1 maps to human chromosome 10, which makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number: 10301-488
Supplier: Bioss
Image Unavailable-10848-478

PP Q 80/100 6 1/8 SS NOC HP

Description: PP Q 80/100 6 1/8 SS NOC HP
Catalog Number: 10848-478
Supplier: Restek
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