Catalog No.
YHJ63301
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Met1-Glu428
Predicted molecular weight
51.20 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
Q9NPH0
Applications
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Form
Lyophilized
Storage buffer
Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Reconstitution
Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping
In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternative Names
Acid phosphatase-like protein 1, ACPL1, PACPL1, ACP6, LPAP, Acid phosphatase 6, lysophosphatidic, Lysophosphatidic acid phosphatase type 6
Identification and functional analysis of lysophosphatidic acid phosphatase type 6 (ACP6) gene in golden pompano (Trachinotusovatus)., PMID:39276813
Structure-Based Design and Development of Phosphine Oxides as a Novel Chemotype for Antibiotics that Dysregulate Bacterial ClpP Proteases., PMID:39221504
Human Genetics of Ventricular Septal Defect., PMID:38884729
Plasma protein changes reflect colorectal cancer development and associated inflammation., PMID:37228491
The expression characteristics and clinical significance of ACP6, a potential target of nitidine chloride, in hepatocellular carcinoma., PMID:36456931
Fisetin promotes osteoblast differentiation and osteogenesis through GSK-3β phosphorylation at Ser9 and consequent β-catenin activation, inhibiting osteoporosis., PMID:34256044
Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound., PMID:31759543
Mutant p53 regulates LPA signaling through lysophosphatidic acid phosphatase type 6., PMID:30914657
Copy Number Variants Are Enriched in Individuals With Early-Onset Obesity and Highlight Novel Pathogenic Pathways., PMID:28605459
Epigenome-wide DNA methylation in hearing ability: new mechanisms for an old problem., PMID:25184702
Crystal structures and biochemical studies of human lysophosphatidic acid phosphatase type 6., PMID:23807634
Stereospecificity of the dehydratase domain of the erythromycin polyketide synthase., PMID:20925342
Isolation, mapping and identification of SNPs for four genes (ACP6, CGN, ANXA9, SLC27A3) from a bovine QTL region on BTA3., PMID:16717448
Tandemly duplicated acyl carrier proteins, which increase polyketide antibiotic production, can apparently function either in parallel or in series., PMID:15583005
Reconstituting modular activity from separated domains of 6-deoxyerythronolide B synthase., PMID:15518537
Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease., PMID:15117819
The hidden steps of domain skipping: macrolactone ring size determination in the pikromycin modular polyketide synthase., PMID:12031664
Novel human and mouse genes encoding an acid phosphatase family member and its downregulation in W/W(V) mouse jejunum., PMID:12010880
Crystal structure of the macrocycle-forming thioesterase domain of the erythromycin polyketide synthase: versatility from a unique substrate channel., PMID:11752428
Rapid degradation of the silkworm diapause hormone by trypsin and its suppression by VAP-map, a synthetic analog of the cuticular peptide of silkworm, Bm ACP-6.7 (VAP-peptide)., PMID:11440114
For research use only. Not for human or drug use.
