You Searched For: 3,5-Dihydroxy-4-methylbenzoic+acid


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Supplier: Thermo Scientific Chemicals
Description: In manufacture of tungsten and tungstates, and in alloys, in fire-proofing fabrics, and as a ceramic pigment
Catalog Number: (89166-052)
Supplier: Enzo Life Sciences
Description: Thiol dye.

Catalog Number: (10087-526)
Supplier: Proteintech
Description: GGPS1(Geranylgeranyl pyrophosphate synthase) belongs to the FPP/GGPP synthase family and catalyzes the synthesis of GGPP, an important molecule responsible for the C20-prenylation of protein and for the regulation of a nuclear hormone receptor. GGPP synthase puri¢ed from bovine brain is reported to be a homo-oligomer (150-195 kDa) with a molecular mass of 37.5 kDa for the monomer.This is consistent with the calculated molecular mass (35 kDa) of mouse and human GGPP synthases .


Catalog Number: (10749-014)
Supplier: Prosci
Description: The Gap junction beta-2 protein (GJB2), also known as Connexin 26, is member of the gap junction protein family which form structures that were shown to consist of cell-to-cell channels that facilitate the transfer of ions and small molecules between cells. Mutations in the GJB2 gene are thought to be responsible for as much as 35-45% of congenital sensorineural hearing loss in some populations. Other mutations in this gene have also been linked to a wide array of skin diseases.


Supplier: Thermo Scientific Chemicals
Description: A histological counterstain. Nuclear Fast Red solution turns cell nuclei red and cytoplasm a pale pink.
Catalog Number: (10496-122)
Supplier: Bioss
Description: ANGEL1 , also known as KIAA0759, is a 670 amino acid protein belonging to the CKR-4 protein family. ANGEL1 is encoded by a gene located on human chromosome 14, which contains about 700 genes and 106 million base pairs, making up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus on chromosome 14 and its fusion via translocation with the chromosome 19 encoded protein BCL3 may be related to B-cell malignancies.


Catalog Number: (10496-120)
Supplier: Bioss
Description: ANGEL1 , also known as KIAA0759, is a 670 amino acid protein belonging to the CKR-4 protein family. ANGEL1 is encoded by a gene located on human chromosome 14, which contains about 700 genes and 106 million base pairs, making up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus on chromosome 14 and its fusion via translocation with the chromosome 19 encoded protein BCL3 may be related to B-cell malignancies.


Catalog Number: (CAAAAL13597-MD)
Supplier: Thermo Scientific Chemicals
Description: A vasodilator

Catalog Number: (10087-512)
Supplier: Proteintech
Description: Protein tags are protein or peptide sequences located either on the C- or N- terminal of the target protein, which facilitates one or several of the following characteristics: solubility, detection, purification, localization and expression. Green fluorescence protein(GFP) is a protein composed of 238 amino acid residues(26.9kDa) derived from the Jellyfish Aequorea victoria, which emits green light(emission peak at 509nm) when excited by blue light(excitation peak at 395nm). GFP has become an invaluable tool in cell biology research, since its intrinsic fluorescence can be visualized in living cells. EGFP contains the double-amino-acid substitutions Phe-64 to Leu and Ser-65 to Thr(previously published as GFPmut1; PMID: 8707053). In contrast to wtGFP, EGFP has a single, strong, red-shifted excitation peak at 488nm. GFPmut1 fluoresces 35-fold more intensely than wtGFP when excited at 488nm, due to an increase in its extinction coefficient(Em). The antibody recognizes the GFP-tag, eGFP tag, eYPF tag, CFP tag or YFP tag fused to either the amino- or carboxy-terminus of targeted proteins in transfected mammalian cells.


Supplier: TCI America
Description: CAS Number: 491-70-3
MDL Number: MFCD00017309
Molecular Formula: C15H10O6
Molecular Weight: 286.24
Purity/Analysis Method: >98.0% (HPLC)
Form: Crystal
Color: Pale Yellow
Melting point (°C): 330
Storage Temperature: 0-10°C
Supplier: TCI America
Description: CAS Number: 144-19-4
MDL Number: MFCD00004681
Molecular Formula: C8H18O2
Molecular Weight: 146.23
Purity/Analysis Method: >97.0% (GC)
Form: Crystal
Color: White
Boiling point (°C): 232
Melting point (°C): 54
Flash Point (°C): 140
Supplier: TCI America
Description: CAS Number: 34338-96-0
MDL Number: MFCD00082583
Molecular Formula: C6H14O2
Molecular Weight: 118.18
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Boiling point (°C): 71
Melting point (°C): 54
Flash Point (°C): 102
Specific rotation [a]20/D: 25 deg (C=1, EtOH)
Catalog Number: (TCN0571-001G)
Supplier: TCI America
Description: CAS Number: 13133-07-8
MDL Number: MFCD00191672
Molecular Formula: C24H42O21
Molecular Weight: 666.58
Purity/Analysis Method: >99.0% (HPLC)
Form: Crystal
Specific rotation [a]20/D: 10 deg (C=4, H2O)

Catalog Number: (10483-870)
Supplier: Bioss
Description: GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.


Supplier: TCI America
Description: CAS Number: 5343-92-0
MDL Number: MFCD00010736
Molecular Formula: C5H12O2
Molecular Weight: 104.15
Purity/Analysis Method: >98.0% (GC)
Form: Clear Liquid
Color: Colorless
Boiling point (°C): 210
Flash Point (°C): 104
Specific Gravity (20/20): 0.97
Supplier: Thermo Scientific Chemicals
Description: (±)-3-(Diethylamino)-1,2-propanediol 97%
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