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You Searched For: 1,4-Diisopropylbenzene


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Image Unavailable-M-1115.0005BA

N feminine(1)U(1/2)oOAeAO-

Catalog Number: (M-1115.0005BA)
Supplier: Bachem Americas
Description: Sequence: H-Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-His-Leu-Leu-Val-Tyr-Ser-OH
Synonym(s): Tetradecapeptide Renin Substrate (horse)#Angiotensinogen (1-14) (horse)#Preangiotensinogen (1-14) (horse)#Angiotensinogen (1-14), porcine
Image Unavailable-ABCA_AB155037-100U

Anti-14-3-3 zeta Rabbit Polyclonal Antibody

Catalog Number: (ABCA_AB155037-100U)
Supplier: Abcam
Description: Rabbit polyclonal to 14-3-3 zeta.

New Product


Image Unavailable-10492-956

Anti-B4GALT7 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10492-956)
Supplier: Bioss
Description: β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a β-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar.
Image Unavailable-ABCA_AB174847-100U

Anti-Caspase-14 Rabbit Monoclonal Antibody [clone: EPR12927]

Supplier: Abcam
Description: Rabbit monoclonal [EPR12927] to Caspase-14.

New Product

Product Image-77215-820

Human 14-3-3 Theta ELISA Kit

Catalog Number: (77215-820)
Supplier: ANTIBODIES.COM LLC
Description: Human 14-3-3 theta ELISA kit is a 90 minute sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the <i>in vitro</i> quantitative determination of human 14-3-3 theta in serum, plasma, and other biological fluids.
Image Unavailable-ABCA_AB181595-1ML

Anti-Cytokeratin 14 Rabbit Monoclonal Antibody [clone: EPR17350]

Supplier: Abcam
Description: Rabbit monoclonal [EPR17350] to Cytokeratin 14 - Cytoskeleton Marker.

New Product

Image Unavailable-ABCA_AB51129-100UG

Anti-14-3-3 zeta Rabbit Polyclonal Antibody

Catalog Number: (ABCA_AB51129-100UG)
Supplier: Abcam
Description: Rabbit polyclonal to 14-3-3 zeta.

New Product


Image Unavailable-ABCA_AB124909-1ML

Anti-14-3-3 Theta + Tau Rabbit Monoclonal Antibody [clone: EPR5123]

Supplier: Abcam
Description: Rabbit monoclonal [EPR5123] to 14-3-3 Theta + Tau.

New Product

Image Unavailable-TCB1485-001G

1,4-Bis(3-hydroxyphenoxy)benzene ≥96.0%

Catalog Number: (TCB1485-001G)
Supplier: TCI America
Description: CAS Number: 5085-95-0
MDL Number: MFCD00142543
Molecular Formula: C18H14O4
Molecular Weight: 294.31
Purity/Analysis Method: >96.0% (GC)
Form: Crystal
Melting point (°C): 126

SDS


Image Unavailable-TCD2190-5G

6,8-Dimethoxy-4-methylquinoline ≥98.0% (by GC, titration analysis)

Supplier: TCI America
Description: CAS Number: 51049-14-0
MDL Number: MFCD00191629
Molecular Formula: C12H13NO2
Molecular Weight: 203.24
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 65

SDS Certificates

Image Unavailable-10492-936

Anti-B4GALT7 Rabbit Polyclonal Antibody

Catalog Number: (10492-936)
Supplier: Bioss
Description: β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a β-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar.
Image Unavailable-10492-954

Anti-B4GALT7 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10492-954)
Supplier: Bioss
Description: β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a β-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar.
Image Unavailable-TCA1288-025G

2-Amino-3-chloro-1,4-naphthoquinone ≥98.0% (by HPLC, total nitrogen)

Supplier: TCI America
Description: CAS Number: 2797-51-5
MDL Number: MFCD00001680
Molecular Formula: C10H6ClNO2
Molecular Weight: 207.61
Purity/Analysis Method: >98.0% (HPLC,N)
Form: Crystal
Melting point (°C): 200

SDS

Product Image-58202-512

Stainless Steel Flat Top Worktable with Undershelf, 14-Gauge Type 304, Eagle MHC™

Supplier: Eagle Group
Description: Tables have a 14 gauge type 304 stainless steel flat top.

Product Image-97058-780

Stainless Steel Worktable with Backsplash and Undershelf, 14-Gauge Type 304, Eagle MHC™

Supplier: Eagle Group
Description: 14 Gauge Type 304 stainless steel top with 4¹/₂" backsplash at rear of table.

Image Unavailable-10492-958

Anti-B4GALT7 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10492-958)
Supplier: Bioss
Description: β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a β-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar.
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