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Catalog Number: (10475-466)
Supplier: Bioss
Description: The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.


Catalog Number: (10475-468)
Supplier: Bioss
Description: The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.


Supplier: TCI America
Description: CAS Number: 111109-77-4
MDL Number: MFCD00210047
Molecular Formula: C8H18O3
Molecular Weight: 162.23
Purity/Analysis Method: >94.0% (GC)
Form: Clear Liquid
Flash Point (°C): 65
Specific Gravity (20/20): 0.90
Supplier: TCI America
Description: CAS Number: 4474-86-6
MDL Number: MFCD00065696
Molecular Formula: C12H14N2O5
Molecular Weight: 266.25
Purity/Analysis Method: >99.0% (T)
Form: Crystal
Melting point (°C): 165
Specific rotation [a]20/D: -6.5 deg (C=1.6, AcOH)

SDS

Supplier: TCI America
Description: CAS Number: 93-17-4
MDL Number: MFCD00001911
Molecular Formula: C10H11NO2
Molecular Weight: 177.20
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Boiling point (°C): 160
Melting point (°C): 65
Flash Point (°C): 250
Catalog Number: (76397-908)
Supplier: Thermo Fisher Scientific
Description: The Nalgene™ multi-tiered portfolio provides bioproduction facilities with a variety of high-quality, sterile storage and transport solutions. Choose the appropriate product necessary to suit any application, through the step-down process and into the cleanroom.


Catalog Number: (10341-262)
Supplier: Bioss
Description: GLUT12 belongs to a family of transporters that catalyze the uptake of sugars through facilitated diffusion. Thirteen different types of glucose/fructose transport carrier proteins designated as Glut 1-13 facilitate glucose/fructose transport across the cell membrane. Individual members of the Glut family have predicted secondary structure characteristic of 12 membrane spanning domains of other transport carriers.


Supplier: TCI America
Description: CAS Number: 703-61-7
MDL Number: MFCD00023939
Molecular Formula: C9H5Cl2N
Molecular Weight: 198.05
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Boiling point (°C): 282
Melting point (°C): 65
Lambda max.: 305 nm (MeOH)
Catalog Number: (89515-634)
Supplier: Abgent
Description: Western Blot: 1:1000


Catalog Number: (89519-982)
Supplier: Abgent
Description: Western Blot: 1:1000


Supplier: TCI America
Description: CAS Number: 9011-14-7
MDL Number: MFCD00134349
Molecular Formula: C5H8O2
Form: Crystal
Color: White
Supplier: Dickies
Description: Dickies® style FP2377, relaxed fit, straight leg.

Supplier: TCI America
Description: CAS Number: 693-36-7
MDL Number: MFCD00026684
Molecular Formula: C42H82O4S
Molecular Weight: 683.17
Purity/Analysis Method: >90.0% (HPLC)
Form: Crystal
Color: White
Melting point (°C): 65
Lambda max.: 410 nm (H2O)
Catalog Number: (101410-644)
Supplier: Electron Microscopy Sciences
Description: The kit consists of two components, equal amount, very low viscosity, (~65 cps), in convenient dispenser top bottles. To prepare the embedding resin, just mix equal amounts of the two components. The resin readily infiltrates into specimen and polymerizes to a clear, hard block overnight at 60°C.

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Catalog Number: (10341-264)
Supplier: Bioss
Description: GLUT12 belongs to a family of transporters that catalyze the uptake of sugars through facilitated diffusion. Thirteen different types of glucose/fructose transport carrier proteins designated as Glut 1-13 facilitate glucose/fructose transport across the cell membrane. Individual members of the Glut family have predicted secondary structure characteristic of 12 membrane spanning domains of other transport carriers.


Catalog Number: (76108-042)
Supplier: Bioss
Description: The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.


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