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035937 Rabbit Anti-GBE1, ID (GBE1, 1,4-alpha-glucan-branching enzyme, Brancher enzyme, Glycogen-branching enzyme)

Specifications
References
Clone Type
Polyclonal
Host
Rabbit
Source
Human
Swiss Prot
Q04446
Isotype
IgG
Grade
Affinity Purified
Applications
E IF WB
Crossreactivity
Hu Mo
Gene ID
2632
Gene #
GBE1
Shipping Temp
Blue Ice
Storage Temp
-20°C
GBE1, 1,4-alpha-glucan-branching enzyme, Brancher enzyme, Glycogen-branching enzyme

GBE1 is a glycogen branching enzyme that catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on the same or a neighboring glycogen chain. Branching of the chains is essential to increase the solubility of the glycogen molecule and, consequently, in reducing the osmotic pressure within cells. Highest level of this enzyme are found in liver and muscle. Mutations in this gene are associated with glycogen storage disease IV (also known as Andersen's disease).

Applications
Suitable for use in Western Blot, Immunofluorescence, ELISA
Recommended Dilution
ELISA: 1:1,000 Western Blot: 1:100-500 Immunofluorescence: 1:10-50
Storage and Stability
May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Immunogen
GBE1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 534~564 amino acids from the Central region of human GBE1.
Form
Supplied as a liquid in PBS, pH 7.2, 0.09% sodium azide.
Purity
Purified by Protein A affinity chromatography.
Specificity
Human, mouse
References
Konstantinidou, A.E., et al. Placenta 29(4):378-381(2008)|Massa, R., et al. Muscle Nerve 37(4):530-536(2008)|Bruno, C., et al. Acta Myol 26(1):75-78(2007)
USBio References
No references available
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