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2-Amino-2-(3-bromophenyl)acetic+acid
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2-Amino-2-(3-bromophenyl)acetic+acid
Supplier:
TCI America
Description:
CAS Number: 25134-21-8
MDL Number: MFCD00167036 Molecular Formula: C10H10O3 Molecular Weight: 178.19 Purity/Analysis Method: >80.0% (GC) Form: Clear Liquid Flash Point (°C): 135 Specific Gravity (20/20): 1.23
Supplier:
BeanTown Chemical
Description:
CAS: 112-80-1; EC No: 204-007-1; MDL No: MFCD00064242; RTECS: RG2275000
Liquid; Linear Formula: CH3(CH2)7CH=CH(CH2)7COOH; Molecular Formula: C18H34O2; MW: 282.47
Melting Point: 13-14°; Boiling Point: 194-195°/1.2 mmHg; Flash point: <gt/>110°C (<gt/>230°F)
Density (g/mL): 0.887; Refractive Index: 1.459
Air Sensitive
Catalog Number:
(10289-792)
Supplier:
Bioss
Description:
ECH1 is a 328 amino acid protein that localizes to both the mitochondrion and the peroxisome and belongs to the hydratase/isomerase superfamily. Existing as a homohexamer, ECH1 is involved in the fatty acid-beta oxidation pathway, specifically functioning to catalyze the isomerization of 3-trans,5-cis-dienoyl-CoA to 2-trans,4-trans-dienoyl-CoA. The gene encoding ECH1 maps to human chromosome 19, which is the genetic home for a number of immunoglobulin superfamily members, including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family and Fc receptors (FcRs).
Catalog Number:
(C-1390.0005BA)
Supplier:
Bachem Americas
Description:
Mix of τ-Bzl (mainly formed) and π-Bzl isomer. CAS Number (τ-isomer): 21929-66-8.
Catalog Number:
(10236-990)
Supplier:
Bioss
Description:
Receptor for retinoic acid. Retinoic acid receptors bind as heterodimers to their target response elements in response to their ligands, all-trans or 9-cis retinoic acid, and regulate gene expression in various biological processes. The RXR/RAR heterodimers bind to the retinoic acid response elements (RARE) composed of tandem 5'-AGGTCA-3' sites known as DR1-DR5. In the absence or presence of hormone ligand, acts mainly as an activator of gene expression due to weak binding to corepressors. In concert with RARG, required for skeletal growth, matrix homeostasis and growth plate function.
Catalog Number:
(101928-950)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 065075-500MG , MDL Number: MFCD09880947
Supplier:
TCI America
Description:
CAS Number: 3685-23-2
MDL Number: MFCD00191730 Molecular Formula: C7H13NO2 Molecular Weight: 143.19 Purity/Analysis Method: >98.0% (GC,T) Form: Crystal
Supplier:
AMBEED, INC
Description:
Bis(oxiran-2-ylmethyl) cyclohexane-1,2-dicarboxylate, Purity: 90% (GC), CAS Number: 5493-45-8, Appearance: Colorless to Yellow Liquid, Storage: Inert atmosphere, Room Temperature, Size: 500g
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Fuchsin (acid), pure, certified
Catalog Number:
(77254-794)
Supplier:
AMBEED, INC
Description:
Ethyl 4-(2-hydroxypropan-2-yl)-2-propyl-1-((2'-(1-trityl-1H-tetrazol-5(4)-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-imidazole-5-carboxylate, Purity: 97% +(isomer mixture), CAS Number: 189400-21-3, Appearance: White to off-white solid, Storage: Sealed in dry, Room Temperature, Size: 250mg
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Cinnamyl chloride 95% (trans-isomers)
Supplier:
AMBEED, INC
Description:
Fuchsin (acid) BS
Catalog Number:
(101094-466)
Supplier:
USP
Description:
It is a mixture of α and β-isomers of calcium gluceptate as the dihydrate.
Supplier:
AMBEED, INC
Description:
Fumaric acid 99+%
Catalog Number:
(76108-560)
Supplier:
Bioss
Description:
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.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
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