Recombinant Human LYPLA1 Protein, GST-tagged
Cat.No. : | LYPLA1-4550H |
Product Overview : | Human LYPLA1 full-length ORF ( AAH08652, 1 a.a. - 230 a.a.) recombinant protein with GST-tag at N-terminal. |
- Specification
- Gene Information
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Description : | Lysophospholipases are enzymes that act on biological membranes to regulate the multifunctional lysophospholipids. The protein encoded by this gene hydrolyzes lysophosphatidylcholine in both monomeric and micellar forms. The use of alternate polyadenylation sites has been found for this gene. There are alternatively spliced transcript variants described for this gene but the full length nature is not known yet. [provided by RefSeq |
Source : | Wheat Germ |
Species : | Human |
Tag : | GST |
Molecular Mass : | 51.04 kDa |
AA Sequence : | MCGNNMSTPLPAIVPAARKATAAVI FLHGLGDTGHGWAEAFAGIRSSHIK YICPHAPVRPVTLNMNVAMPSWFDI IGLSPDSQEDESGIKQAAENIKALI DQEVKNGIPSNRIILGGFSQGGALS LYTALTTQQKLAGVTALSCWLPLRA SFPQGPIGGANRDISILQCHGDCDP LVPLMFGSLTVEKLKTLVNPANVTF KTYEGMMHSSCQQEMMDVKQFIDKL LPPID |
Applications : | Enzyme-linked Immunoabsorbent Assay Western Blot (Recombinant protein) Antibody Production Protein Array |
Notes : | Best use within three months from the date of receipt of this protein. |
Storage : | Store at -80 centigrade. Aliquot to avoid repeated freezing and thawing. |
Storage Buffer : | 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer. |
Gene Name : | LYPLA1 lysophospholipase I [ Homo sapiens ] |
Official Symbol : | LYPLA1 |
Synonyms : | LYPLA1; lysophospholipase I; acyl-protein thioesterase 1; LPL1; LPL-I; lysoPLA I; lysophospholipase 1; acyl-protein thioesterase-1; lysophospholipid-specific lysophospholipase; APT-1; hAPT1; LYSOPLA; |
Gene ID : | 10434 |
mRNA Refseq : | NM_006330 |
Protein Refseq : | NP_006321 |
MIM : | 605599 |
UniProt ID : | O75608 |
Products Types
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◆ Lysates | ||
LYPLA1-4589HCL | Recombinant Human LYPLA1 293 Cell Lysate | +Inquiry |
Related Gene
For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (7)
Ask a questionGenetic mutations in LYPLA1 can lead to dysregulation of lipid metabolism and protein modification.
Altered LYPLA1 activity is linked to various diseases, including metabolic and neurodegenerative disorders.
Targeting LYPLA1 could provide new strategies for treating diseases related to lipid metabolism and protein modification.
LYPLA1 works with other lipid metabolism enzymes, coordinating lipid modification and signaling pathways.
LYPLA1, a lysophospholipase, is involved in lipid metabolism, crucial for maintaining cellular lipid balance.
LYPLA1 is involved in signal transduction processes by modulating the lipidation status of signaling proteins.
It plays a role in protein modification, particularly in depalmitoylation, affecting protein function and localization.
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