4281 Results for: "cis-1,3-Dibenzyl-2-oxo-4,5-imidazolidinecarboxylic acid"

Supplier: Thermo Scientific Chemicals

3-Oxoglutaric acid 97%

Supplier: TCI America

CAS Number: 1623-08-1
MDL Number: MFCD00004775
Molecular Formula: C14H15O4P
Molecular Weight: 278.24
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Color: White
Melting point (°C): 81
Storage Temperature: <0°C

Supplier: Thermo Scientific Chemicals

Mast cell stabilizer that prevents release of histamine from mast cells

Supplier: Bioss

RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.

Supplier: Bioss

RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.

Supplier: MilliporeSigma

Cell-permeable fluorogenic probe that is useful for the detection of reactive oxygen species (ROS) and nitric oxide (NO) and for the determination of the overall oxidative stress in toxicological phenomena.

Supplier: Bioss

RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.

Supplier: TCI America

CAS Number: 94-60-0
MDL Number: MFCD00001460
Molecular Formula: C10H16O4
Molecular Weight: 200.23
Purity/Analysis Method: >92.0% (GC)
Form: Clear Liquid
Boiling point (°C): 263
Flash Point (°C): 94
Freezing point (°C): 13

Supplier: Bioss

RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.

Supplier: TCI America

CAS Number: 2451-84-5
MDL Number: MFCD00059667
Molecular Formula: C20H22O4
Molecular Weight: 326.39
Purity/Analysis Method: >95.0% (GC)
Form: Crystal
Freezing point (°C): 36

Supplier: Bioss

RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.

Supplier: Bioss

RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.

Supplier: Thermo Scientific Chemicals

Supplier: TCI America

CAS Number: 2746-19-2
Molecular Formula: C9H8O3
Molecular Weight: 164.16
Purity/Analysis Method: >97.0% (GC,T)
Form: Crystal
Melting point (°C): 144

Supplier: Proteintech

NDUFS6(NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial) is also named as CI-13kD-A, NADH-ubiquinone oxidoreductase 13 kDa-A subunit and belongs to the complex I NDUFS6 subunit family.It is an accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis.

Supplier: Bioss

RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.

Supplier: Thermo Scientific Chemicals

Collagen stain for connective tissue

Supplier: Thermo Scientific Chemicals

DNA loading dye used to prepare markers and samples for loading on agarose or polyacrylamide gels in molecular biology protocols.

Supplier: TCI America

CAS Number: 37031-29-1
MDL Number: MFCD00066218
Molecular Formula: C9H14O6
Molecular Weight: 218.21
Purity/Analysis Method: >95.0% (GC)
Form: Clear Liquid
Boiling point (°C): 139
Flash Point (°C): 110
Specific Gravity (20/20): 1.19
Specific rotation [a]20/D: -54 deg (neat)

Supplier: Prosci

Interleukin-15 receptor subunit alpha, also known as Il15ra, is a high-affinity receptor for interleukin-15. Il15ra associates as a heterotrimer with the IL-2 receptor beta and gamma subunits (Common gamma chain, or gamma c) to initiate signal transduction. It can signal both in cis and trans where IL15R from one subset of cells presents IL15 to neighboring IL2RG-expressing cells. Il15ra is expressed in special cells including a wide variety of Tand B cells and non-lymphoid cells. Human Il15ra shares 45% amino acid sequence homology with the mouse form of the receptor. Eight isoforms of IL-15 R alpha mRNA have been identified, resulting from alternative splicing events involving different exons.Interleukin 15 (IL-15) is a cytokine that regulates T cell and natural killer cell activation and proliferation. IL-15 binds to the alpha subunit of the IL15 receptor (IL-15RA) with high affinity. IL-15 also binds to the beta and gamma chains of the IL-2 receptor, but not the alpha subunit of the IL2 receptor. IL-15 is structurally and functionally related to IL-2. Both cytokines share some subunits of receptors, allowing them to compete for and negatively regulate each other's activity. The number of CD8+ memory T cells is controlled by a balance between IL-15 and IL-2. Despite their many overlapping functional properties, IL-2 and IL-15 are, in fact, quite distinct players in the immune system. IL-15 is constitutively expressed by a wide variety of cell types and tissues, including monocytes, macrophages and DCs.

Supplier: Thermo Scientific Chemicals

Powder

Supplier: Thermo Scientific Chemicals

A tracking dye for DNA sequencing

Supplier: TCI America

CAS Number: 7396-41-0
MDL Number: MFCD00142532
Molecular Formula: C7H6O4S3
Molecular Weight: 250.30
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Melting point (°C): 88

Supplier: TCI America

CAS Number: 149-45-1
MDL Number: MFCD00007473
Molecular Formula: C6H6O8S2
Molecular Weight: 314.19
Purity/Analysis Method: >98.0% (T)
Form: Crystal

Supplier: Thermo Scientific Chemicals

1,2-Dihydroxybenzene-3,5-disulfonic acid disodium salt monohydrate 97%

Supplier: TCI America

CAS Number: 1058-92-0
MDL Number: MFCD00003941
Molecular Formula: C16H11ClN2O9S2
Molecular Weight: 518.80
Form: Crystal
Color: Deep Yellow

Supplier: TCI America

CAS Number: 37031-30-4
MDL Number: MFCD00040504
Molecular Formula: C9H14O6
Molecular Weight: 218.21
Purity/Analysis Method: >95.0% (GC)
Form: Clear Liquid
Flash Point (°C): 135
Specific Gravity (20/20): 1.19
Specific rotation [a]20/D: 54 deg (neat)

Supplier: TCI America

CAS Number: 469-77-2
MDL Number: MFCD00059059
Molecular Formula: C17H28O6
Molecular Weight: 328.41
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 145
Specific rotation [a]20/D: -13 deg (C=3, EtOH)

Supplier: MilliporeSigma

Cas Number 149-45-1, (Tiron) Metal Indicator

Supplier: TCI America

CAS Number: 761446-45-1
MDL Number: MFCD03789252
Molecular Formula: C16H21BN2O2
Molecular Weight: 284.17
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Melting point (°C): 89