Product Name
GALC Recombinant Rabbit Monoclonal Antibody [PSH04-32] - BSA and Azide free
Antibody Type
Recombinant Rabbit monoclonal Antibody
Immunogen
Recombinant protein within human GALC aa 1-500 / 685.
Target Molecular Weight
Predicted band size: 77 kDa
Positive Control
293T cell lysate, A375 cell lysate, A549 cell lysate, SH-SY5Y cell lysate, HaCaT cell lysate, human brain tissue, human liver cancer tissue.
Storage Instructions
Store at 2-8℃. Avoid freeze.
Purification Method
Protein A affinity purified.
Function
Galactosylceramidase (or galactocerebrosidase), EC 3.2.1.46, is an enzyme that removes galactose from ceramide derivatives (galactosylceramides) by catalysing the hydrolysis of galactose ester bonds of galactosylceramide, galactosylsphingosine, lactosylceramide, and monogalactosyldiglyceride. It is a lysosomal protein, encoded in humans by the GALC gene. Mutations in this gene have been associated with Krabbe disease, also known as galactosylceramide lipidosis.
Background References
1. Senkevich K et al. GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson\'s disease. Brain. 2023 May
2. Tian G et al. rAAV2-Mediated Restoration of GALC in Neural Stem Cells from Krabbe Patient-Derived iPSCs. Pharmaceuticals (Basel). 2023 Apr
Synonyms
Gacy antibody
Galactocerebrosidase antibody
Galactocerebroside beta galactosidase antibody
Galactocerebroside beta-galactosidase antibody
Galactosylceramidase antibody
Galactosylceramide beta galactosidase antibody
Galactosylceramide beta-galactosidase antibody
galactosylceraminidase antibody
GALC antibody
GALC_HUMAN antibody
Expand
Gacy antibody
Galactocerebrosidase antibody
Galactocerebroside beta galactosidase antibody
Galactocerebroside beta-galactosidase antibody
Galactosylceramidase antibody
Galactosylceramide beta galactosidase antibody
Galactosylceramide beta-galactosidase antibody
galactosylceraminidase antibody
GALC antibody
GALC_HUMAN antibody
GALCERase antibody
Twitcher antibody
Collapse
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This data was developed using HA722115, the same antibody clone in a different buffer formulation.
Western blot analysis of GALC on different lysates with Rabbit anti-GALC antibody (HA722115) at 1/2,000 dilution.
Lane 1: 293T cell lysate (20 µg/Lane)
Lane 2: A375 cell lysate (20 µg/Lane)
Lane 3: A549 cell lysate (20 µg/Lane)
Lane 4: SH-SY5Y cell lysate (20 µg/Lane)
Predicted band size: 77 kDa
Observed band size: 48 kDa
Exposure time: 3 minutes; ECL: K1801;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA722115) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
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This data was developed using HA722115, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human brain tissue with Rabbit anti-GALC antibody (HA722115) at 1/200 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA722115) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
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This data was developed using HA722115, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human liver cancer tissue with Rabbit anti-GALC antibody (HA722115) at 1/200 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA722115) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"