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OriGene Antibodies in recent publications
A common polymorphism in the LDL receptor gene has multiple effects on LDL receptor function Hum. Mol. Genet., Apr 2013; 22: 1424 - 1431. [anti-DDK]

Excitotoxicity Upregulates SARM1 Protein Expression and Promotes Wallerian-Like Degeneration of Retinal Ganglion Cells and Their Axons Invest. Ophthalmol. Vis. Sci., Apr 2013; 54: 2771 - 2780. [SARM1]

Modulation of TET2 expression and 5-methylcytosine oxidation by the CXXC domain protein IDAX Nature 497, 122-126 doi:10.1038/nature12052 [anti-DDK]

Natriuretic Peptide Receptor-3 Gene (NPR3): Nonsynonymous Polymorphism Results in Significant Reduction in Protein Expression Because of Accelerated Degradation Circ Cardiovasc Genet, Apr 2013; 6: 201 - 210. [NPR3]

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Home All anti-ABCA1 antibodies

Anti-ABCA1 Phospho Antibody EPR2485

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Specifications Related Products Conjugation/Bulk FAQs
SKU Description Amount Price Availability*  
TA310159
  • Rabbit Monoclonal antibody against ABCA1 (pS2054) (Phospho-specific)
100ul $325 3-7 Days Add to Shopping Cart
WB(1)
IF(1)
Gene NameHomo sapiens ATP-binding cassette, sub-family A (ABC1), member 1 (ABCA1)
Synonyms:ABC-1; ABC1; CERP; HDLDT1; TGD
ImmunogenA phospho specific peptide corresponding to residues surrounding serine 2054 of human ABCA1 was used as an immunogen. This antibody only detects ABCA1 phosphorylated at serine 2054.
BufferStore at -20 °C. Buffer: Antibody buffer, sodium azide, glycerol, and BSA. Stable for 12 months from date of receipt.
Clone NameEPR2485 Isotype
Species ReactivityHuman, Mouse Concentration
Guaranteed Application *WB, IF Suggested DilutionsWB: 1:1,000-10,000; IHC 1:50 - 100; FC: 1:10 - 100;
BackgroundABCA1 is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes, and are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. With cholesterol as its substrate, ABCA1 functions as a cholesterol efflux pump in the cellular lipid removal pathway. Mutations in this protein have been associated with Tangier's disease and familial high-density lipoprotein deficiency (1). It has been shown that Ser-1042 and Ser-2054, located in the nucleotide binding domains of ABCA1, are major phosphorylation sites for PKA. Phosphorylation of Ser-2054 within the nucleotide binding domain 2 was found to be particularly important for ApoA-I-dependent phospholipid efflux activity mediated by ABCA1 (2).
Related Pathway

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WB Image
Western blot analysis on SH-SY5Y cell lysates using anti-Phospho-ABCA1 (pS2054) RabMAb. Cells were either (A) untreated (B) treated with Okadaic Acid and Calyculin A.<br>Note: Primary antibody was diluted with 1% BSA.
IF Image
Immunofluorescent analysis of SH-SY5Y cells treated with Okadaic Acid and Calyculin A using anti-Phospho-ABCA1 (pS2054) RabMAb

 

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