Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 009020-25G , MDL Number: MFCD00007328
Supplier:
AMBEED, INC
Description:
3-(Trifluoromethyl)benzenethiol, Purity: 98%, CAS Number: 937-00-8, Appearance: Liquid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 5g
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
EDTA tripotassium salt dihydrate 99+%
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
α,4-Dichlorotoluene 99+%
Supplier:
Thermo Fisher Scientific
Description:
Enhancing the advanced features of the Heracell 160i CO₂ incubator, the Cell Locker System is a breakthrough for cultures in frequently opened or shared use incubators.
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 020555-5G , MDL Number: MFCD06797751
Supplier:
TCI America
Description:
CAS Number: 80522-42-5
MDL Number: MFCD00009913 Molecular Formula: C10H21F3O3SSi Molecular Weight: 306.42 Purity/Analysis Method: >98.0% (T) Form: Clear Liquid Color: Colorless Boiling point (°C): 87 Flash Point (°C): 100 Specific Gravity (20/20): 1.14
Catalog Number:
(470146-288)
Supplier:
Medegen Medical Products, LLC
Description:
Shatterproof Polypropylene.
Catalog Number:
(10270-108)
Supplier:
Bioss
Description:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. 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. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. 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.
Catalog Number:
(10278-358)
Supplier:
Bioss
Description:
PTCHD3 is a 767 amino acid multi-pass membrane protein that localizes to the midpiece of the sperm tail, where it is implicated in sperm function and development. A member of the patched family, PTCHD3 contains one SSD (sterol-sensing) domain and is encoded by a gene that maps to human chromosome 10p12.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number:
(101933-602)
Supplier:
Matrix Scientific
Description:
MF=C9H9Br MW=197.08 Cas=1798-85-2 MDL=MFCD01070823 500Mg
Supplier:
AMBEED, INC
Description:
1-Bromo-4-(tert-butyl)-2-iodobenzene 95%
Supplier:
AMBEED, INC
Description:
4-Chloro-3-(trifluoromethyl)benzenesulfonyl Chloride, Purity: 98%, CAS number: 32333-53-2, Appearance: White to Yellow Solid, Storage: Inert atmosphere, Room Temperature, Size: 1G
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
α,4-Dibromotoluene 98%
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
4-(4-Nitrophenylazo)resorcinol 90%
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