Recombinant Human Alpha 1 Acid Glycoprotein/AGP (denatured) (ab109931)
Key features and details
- Expression system: Escherichia coli
- Purity: > 90% SDS-PAGE
- Suitable for: SDS-PAGE
Description
-
Product name
Recombinant Human Alpha 1 Acid Glycoprotein/AGP (denatured)
See all Alpha 1 Acid Glycoprotein/AGP proteins and peptides -
Purity
> 90 % SDS-PAGE.
ab109931 is purified using conventional chromatography techniques. -
Expression system
Escherichia coli -
Accession
-
Protein length
Full length protein -
Animal free
No -
Nature
Recombinant -
-
Species
Human -
Sequence
MQIPLCANLVPVPITNATLDQITGKWFYIASAFRNEEYNKSVQEIQATFF YFTPNKTEDTIFLREYQTRQDQCIYNTTYLNVQRENGTISRYVGGQEHFA HLLILRDTKTYMLAFDVNDEKNWGLSVYADKPETTKEQLGEFYEALDCLR IPKSDVVYTDWKKDKCEPLEKQHEKERKQEEGES -
Predicted molecular weight
22 kDa -
Amino acids
19 to 201
-
Associated products
Specifications
Our Abpromise guarantee covers the use of ab109931 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
-
Applications
SDS-PAGE
-
Form
Liquid -
Concentration information loading...
Preparation and Storage
-
Stability and Storage
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
pH: 8.00
Constituents: 2.4% Urea, 0.32% Tris HCl, 5% Glycerol (glycerin, glycerine)
General Info
-
Alternative names
- A1AG1_HUMAN
- AGP
- AGP 1
see all -
Function
Appears to function in modulating the activity of the immune system during the acute-phase reaction. -
Tissue specificity
Expressed by the liver and secreted in plasma. -
Sequence similarities
Belongs to the calycin superfamily. Lipocalin family. -
Cellular localization
Secreted. - Information by UniProt
Images
Protocols
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
Datasheets and documents
References (0)
ab109931 has not yet been referenced specifically in any publications.