Human HTT Protein, MBP, His Tag (MALS verified)
Huntingtin is the protein coded for by the HTT gene. Autosomal dominant mutation in the Huntingtin (Htt) protein is the cause of Huntington’s Disease (HD) . In HD, the polyglutamine (polyQ) domain in the N-terminal sequenceof the protein is expanded beyond a threshold of 36 glutamines. mutant polyQ expansion strongly correlates in an inverse manner to disease age of onset.
Product Specifications
Background
Specifications
Accession Number
P42858-1
Expression Region
Met 1 - Glu 82
Host
E. coli
Target
HTT
Conjugation
Unconjugated
Tag
N-MBP & C-10xHis
Source
Human
Stability
Endotoxin
1.0 EU per μg
Purity
95%
Format
Powder
Buffer
20 mM HEPES, 150 mM NaCl, pH7.5
Additives
Trehalose
Molecular Weight
52.7 kDa
Additionnal Information
Please see 'Shipping-and-Payments' sheet. Website: https://www.acrobiosystems.com/support/shipping-and-payments
Shipping Conditions
RT
Storage Conditions
-20°C
Package Size
500ug*1
Product Datasheet
https://console.acrobiosystems.com/public/product/pdf/ds/HTT-H51M5.pdf
Host or Source
E. coli
Species
Human
Protein ID
P42858-1
Preservative
Trehalose
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