You Searched For: 4-Bromo-2,2-diphenylbutyric+acid


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Supplier: TCI America
Description: [for Biochemical Research]
CAS Number: 144110-43-0
MDL Number: MFCD00153929
Molecular Formula: C14H13BrClNO7
Molecular Weight: 521.79
Purity/Analysis Method: >98.0% (HPLC)
Form: Crystal
Specific rotation [a]20/D: -69 deg (C=1, 50%DMF)
Storage Temperature: >-20°C
Supplier: Peprotech
Description: CD40, a member of the TNF receptor superfamily, is a cell surface protein expressed on B cells, dendritic cells, monocytes, thymic epithelial cells and, at low levels, on T cells. Signaling though CD40 plays an important role in the proliferation and differentiation of B cells, and is critical for immunoglobulin (Ig) class switching. The membrane-anchored CD40-Ligand is expressed almost exclusively on activated CD4+ T lymphocytes. Failure to express CD40L leads to “immunodeficiency with hyper-IgM”, a disease characterized by failure to produce IgG, IgA and IgE. The human CD40L gene codes for a 261 amino acid type II transmembrane protein, which contains a 22 amino acid cytoplasmic domain, a 24 amino acid transmembrane domain, and a 215 amino acid extracellular domain. The soluble form of CD40L is an 18 kDa protein comprising the entire TNF homologous region of CD40L and is generated in vivo by an intracellular proteolytic processing of the full length CD40L. Recombinant Human sCD40 ligand is a 16.3 kDa protein containing 149 amino acid residues comprising the receptor binding TNF-like domain of CD40L.

Supplier: TCI America
Description: CAS Number: 6065-63-0
MDL Number: MFCD00026840
Molecular Formula: C13H24O4
Molecular Weight: 244.33
Purity/Analysis Method: >97.0% (GC)
Form: Clear Liquid
Boiling point (°C): 249
Specific Gravity (20/20): 0.96

SDS

Catalog Number: (10664-986)
Supplier: Bioss
Description: The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Jul 2008].


Supplier: TCI America
Description: Ethyl (4-Bromobenzoyl)Acetate, Purity: >98.0%(GC), Cas no: 26510-95-2, MF: C11H11BrO3, MW: 271.11, Synonyms: (4-Bromobenzoyl)acetic Acid Ethyl Ester, 3-(4-Bromophenyl)-3-oxopropionic Acid Ethyl Ester, Ethyl 3-(4-Bromophenyl)-3-oxopropionate, Size: 1G

Catalog Number: (10108-306)
Supplier: Prosci
Description: ASL is a member of the lyase 1 family. The protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in its gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described.


Catalog Number: (CAAA42773-AE)
Supplier: Thermo Scientific Chemicals
Description: Xylenol orange tetrasodium salt 0.1% (w/v) in aqueous solution

Supplier: Thermo Scientific Chemicals
Description: Substrate for beta-glucuronidase
Catalog Number: (CAPIPA5-18273)
Supplier: Thermo Scientific
Description: This antibody is predicted to react with canine, mouse and porcine based on sequence homology. This gene encodes a 42.6 kD subunit of dynactin, a macromolecular complex consisting of 10-11 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. It is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, chromosome movement, nuclear positioning, and axonogenesis. This subunit is present in 8-13 copies per dynactin molecule, and is the most abundant molecule in the dynactin complex. It is an actin-related protein, and is approximately 60% identical at the amino acid level to conventional actin.


Supplier: TCI America
Description: CAS Number: 16732-70-0
MDL Number: MFCD00022701
Molecular Formula: C11H10BrNO2
Molecular Weight: 268.11
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Melting point (°C): 165
Supplier: TCI America
Description: 4-Bromobutyl Acetate, Purity: >97.0%(GC), CAS Number: 4753-59-7, Molecular Formula: C6H11BrO2, Molecular Weight: 195.06, Synonyms: Acetic Acid 4-Bromobutyl Ester, Size: 5G

Catalog Number: (CA80050-480)
Supplier: MilliporeSigma
Description: X-GlcA ((5-bromo-4-chloro-3-indolyl-ß-D-glucuronide) cyclohexylammonium salt)


Catalog Number: (10108-304)
Supplier: Prosci
Description: ASL is a member of the lyase 1 family. The protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in its gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described.


Supplier: TCI America
Description: CAS Number: 5470-70-2
MDL Number: MFCD00006340
Molecular Formula: C8H9NO2
Molecular Weight: 151.17
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Boiling point (°C): 160
Melting point (°C): 34
Flash Point (°C): 103
Catalog Number: (89517-856)
Supplier: Abgent
Description: Western Blot: 1:1000


Supplier: Thermo Scientific Chemicals
Description: (±)-4-Bromomandelic acid 98+%
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