Phospho-ABCA1 (Ser2054) Rabbit pAb
Cat#:DPA05370应用:WB,ICC/IF
Product Name: | Phospho-ABCA1 (Ser2054) Rabbit pAb |
Cat No.: | DPA05370 |
Clonality: | Polyclonal |
Species Reactivity: | Human, Mouse |
Tested Applications: | WB,ICC/IF |
Recommended Dilution: | WB: 1:2000-1:10000 ICC/IF: 1:100 |
Size: | 30ul 50ul 100uL |
Format: | Liquid |
Source: | Rabbit |
Purification Method: | Affinity Purification |
Isotype: | IgG |
Conjugate: | Un-conjugated |
Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
Immunogen: | A synthetic phosphopeptide corresponding to residues surrounding Ser2054 of human ABCA1 |
Calculated Molecular Weight: | 254 kDa |
Observed Molecular Weight: | 254 kDa |
GenBank Accession Number: | O95477 |
Gene ID (NCBI): | 19 |
Synonyms: | TGD; ABC1; CERP; ABC-1; HDLDT1; HPALP1; HDLCQTL13 |
Background: | The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes 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, this protein functions as a cholesteral efflux pump in the cellular lipid removal pathway. Mutations in both alleles of this gene cause Tangier disease and familial high-density lipoprotein (HDL) deficiency. [provided by RefSeq, Sep 2019] |
Category: | Primary Ab |