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Home Antibody All anti-GBE1 antibodies

Anti-GBE1 TRUEMAB Antibody Clone OTI3B4

TrueMAB™ Antibodies - Made against Authentic Protein Antigens

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Specifications Citations (1) Related Products Product Documents
SKU Description Amount Price Availability*  
TA500801 GBE1 mouse monoclonal antibody, clone OTI3B4 (formerly 3B4) 100ul $325 In Stock
LC400056 GBE1 HEK293T cell transient overexpression lysate (as WB positive control) 20ug $50 In Stock
CF500801 Carrier-free (BSA/glycerol-free) GBE1 mouse monoclonal antibody, clone OTI3B4 (formerly 3B4) 100ug $450 3-4 weeks

Buy any antibody of 100ul or more, get a free package of 3 loading control antibody samples. View Details Add to Shopping Cart

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WB(3)
IP(1)
IHC(5)

OriGene Data

ImmunogenFull length human recombinant protein of human GBE1 (NP_000149) produced in HEK293T cell.
Clone NameClone OTI3B4 IsotypeIgG2a
Species ReactivityHuman Concentration1 mg/ml
Guaranteed Application *WB, IHC, IP Suggested DilutionsWB 1:2000, IHC 1:50, IP 2ug/500ul
Predicted MW Explanation 80.3 kDa
BufferPBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Purification Purified from mouse ascites fluids by affinity chromatography

Reference Data

Target NameHomo sapiens glucan (1,4-alpha-), branching enzyme 1 (GBE1)
Alternative NameAPBD; GBE; GSD4
Database LinkNP_000149
Entrez Gene 2632 Human
FunctionThe protein encoded by this gene 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). [provided by RefSeq].
Related PathwayDruggable Genome Starch and sucrose metabolismMetabolic pathways

* Availability is in business days
* OriGene provides validated application data and protocol, with money back guarantee.

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY GBE1 (RC204152, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-GBE1.
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Western blot analysis of extracts (10ug) from 2 different cell lines by using anti-GBE1 monoclonal antibody.(1:200)
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Figure from citation: Western Blot of GBE1 protein level by using anti-GBE1 antibody in mouse muscle extracts obtained from Gbe1-/-. Gbe1+/- and Gbe1+/+ embryos. View Citation
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Immunohistochemical staining of paraffin-embedded Human Kidney tissue within the normal limits using anti-GBE1 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100C for 10min, TA500801)
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Immunohistochemical staining of paraffin-embedded Human liver tissue within the normal limits using anti-GBE1 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100C for 10min, TA500801)
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Immunohistochemical staining of paraffin-embedded Carcinoma of Human liver tissue using anti-GBE1 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100C for 10min, TA500801)
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Immunohistochemical staining of paraffin-embedded Human pancreas tissue within the normal limits using anti-GBE1 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100C for 10min, TA500801)
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Immunohistochemical staining of paraffin-embedded Carcinoma of Human prostate tissue using anti-GBE1 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100C for 10min, TA500801)
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Immunoprecipitation(IP) of GBE1 by using TrueMab monoclonal anti-GBE1 antibodies (Negative control: IP without adding anti-GBE1 antibody.). For each experiment, 500ul of DDK tagged GBE1 overexpression lysates (at 1:5 dilution with HEK293T lysate), 2ug of anti-GBE1 antibody and 20ul (0.1mg) of goat anti-mouse conjugated magnetic beads were mixed and incubated overnight. After extensive wash to remove any non-specific binding, the immuno-precipitated products were analyzed with rabbit anti-DDK polyclonal antibody.
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