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Anti-GBE1 TRUEMAB Antibody Clone OTI1D11

TrueMAB™ Antibodies - Made against Authentic Protein Antigens

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Specifications Citations (1) Related Products Product Documents
SKU Description Amount Price Availability*  
TA500829 GBE1 mouse monoclonal antibody, clone OTI1D11 (formerly 1D11) 100ul
30ul
$379 In Stock
LC400056 GBE1 HEK293T cell transient overexpression lysate (as WB positive control) 20ug $50 In Stock
CF500829 Carrier-free (BSA/glycerol-free) GBE1 mouse monoclonal antibody, clone OTI1D11 (formerly 1D11) 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(4)
IP(1)
IHC(3)
IF(2)
FC(2)

OriGene Data

ImmunogenFull length human recombinant protein of human GBE1 (NP_000149) produced in HEK293T cell.
Clone NameClone OTI1D11 IsotypeIgG1
Species ReactivityHuman Concentration1.1 mg/ml
Guaranteed Application *WB, IHC, IF, IP, FC Suggested DilutionsWB 1:500~2000, IHC 1:50, IF 1:50~100, FLOW 1:100, 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 (35ug) from 9 different cell lines by usin g anti-GBE1 monoclonal antibody (HepG2: human; HeLa: human; SVT2: mouse; A549: human; COS7: monkey; Jurkat: human; MDCK: canine; PC12: rat; MCF7: human).
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Western blot analysis of extracts (10ug) from 10 Human tissue by using anti-GBE1 monoclonal antibody at 1:500 (1: Testis; 2: Omentum; 3: Uterus; 4: Breast; 5: Brain; 6: Liver; 7: Ovary; 8: Thyroid gland; 9: colon;10: spleen).
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Figure from citation: Western Blot of GBE protein level by using anti-GBE antibody in mouse muscle extracts obtained from Gbe1-/-. Gbe1+/- and Gbe1+/+ embryos. View Citation
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Immunohistochemical staining of paraffin-embedded Human colon tissue within the normal limits using anti-GBE1 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100C for 10min, TA500829)
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Immunohistochemical staining of paraffin-embedded Human Ovary tissue within the normal limits using anti-GBE1 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100C for 10min, TA500829)
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Immunohistochemical staining of paraffin-embedded Human endometrium tissue within the normal limits using anti-GBE1 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100C for 10min, TA500829)
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Anti-GBE1 mouse monoclonal antibody (TA500829) immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY GBE1(RC204152).
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Immunofluorescent staining of HepG2 cells using anti-GBE1 mouse monoclonal antibody (TA500829).
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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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HEK293T cells transfected with either RC204152 overexpress plasmid(Red) or empty vector control plasmid(Blue) were immunostained by anti-GBE1 antibody(TA500829), and then analyzed by flow cytometry.
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Flow cytometric Analysis of Jurkat cells, using anti-GBE1 antibody(TA500829),(Red), compared to a nonspecific negative control antibody,(Blue).
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