Anti-PTDSS1 Antibody (CAB13065)
- SKU:
- CAB13065
- Product type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Metabolism
Frequently bought together:
Description
Antibody Name: | Anti-PTDSS1 Antibody |
Antibody SKU: | CAB13065 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB |
Reactivity: | Human |
Host Species: | Rabbit |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-70 of human PTDSS1 (NP_055569.1). |
Application: | WB |
Recommended Dilution: | WB 1:500 - 1:2000 |
Reactivity: | Human |
Positive Samples: | Raji |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-70 of human PTDSS1 (NP_055569.1). |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | MASC VGSR TLSK DDVN YKMH FRMI NEQQ VEDI TIDF FYRP HTIT LLSF TIVS LMYF AFTR DDSV PEDN IW |
Gene ID: | 9791 |
Uniprot: | P48651 |
Cellular Location: | Endoplasmic reticulum membrane, Multi-pass membrane protein |
Calculated MW: | 56kDa |
Observed MW: | 55kDa |
Synonyms: | PTDSS1, LMHD, PSS1, PSSA |
Background: | The protein encoded by this gene catalyzes the formation of phosphatidylserine from either phosphatidylcholine or phosphatidylethanolamine. Phosphatidylserine localizes to the mitochondria-associated membrane of the endoplasmic reticulum, where it serves a structural role as well as a signaling role. Defects in this gene are a cause of Lenz-Majewski hyperostotic dwarfism. Two transcript variants encoding different isoforms have been found for this gene. |
UniProt Protein Function: | PTDSS1: Catalyzes a base-exchange reaction in which the polar head group of phosphatidylethanolamine (PE) or phosphatidylcholine (PC) is replaced by L-serine. In membranes, PTDSS1 catalyzes mainly the conversion of phosphatidylcholine. Also converts, in vitro and to a lesser extent, phosphatidylethanolamine. Belongs to the phosphatidyl serine synthase family. |
UniProt Protein Details: | Protein type:EC 2.7.8.29; Membrane protein, integral; Mitochondrial; Lipid Metabolism - glycerophospholipid; Membrane protein, multi-pass; Transferase Chromosomal Location of Human Ortholog: 8q22 Cellular Component: endoplasmic reticulum membrane; integral to membrane; membrane Molecular Function:transferase activity Biological Process: phosphatidylserine biosynthetic process; phospholipid biosynthetic process Disease: Lenz-majewski Hyperostotic Dwarfism |
NCBI Summary: | The protein encoded by this gene catalyzes the formation of phosphatidylserine from either phosphatidylcholine or phosphatidylethanolamine. Phosphatidylserine localizes to the mitochondria-associated membrane of the endoplasmic reticulum, where it serves a structural role as well as a signaling role. Defects in this gene are a cause of Lenz-Majewski hyperostotic dwarfism. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014] |
UniProt Code: | P48651 |
NCBI GenInfo Identifier: | 1346881 |
NCBI Gene ID: | 9791 |
NCBI Accession: | P48651.1 |
UniProt Secondary Accession: | P48651,Q9BUQ5, B4DE85, E5RFC5, |
UniProt Related Accession: | P48651 |
Molecular Weight: | 34,579 Da |
NCBI Full Name: | Phosphatidylserine synthase 1 |
NCBI Synonym Full Names: | phosphatidylserine synthase 1 |
NCBI Official Symbol: | PTDSS1 |
NCBI Official Synonym Symbols: | LMHD; PSS1; PSSA |
NCBI Protein Information: | phosphatidylserine synthase 1 |
UniProt Protein Name: | Phosphatidylserine synthase 1 |
UniProt Synonym Protein Names: | Serine-exchange enzyme I |
Protein Family: | Phosphatidylserine synthase |
UniProt Gene Name: | PTDSS1 |
UniProt Entry Name: | PTSS1_HUMAN |