Anti-PCYT1A Antibody (CAB16943)
- SKU:
- CAB16943
- Product type:
- Antibody
- Reactivity:
- Human
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
Frequently bought together:
Description
Antibody Name: | Anti-PCYT1A Antibody |
Antibody SKU: | CAB16943 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB |
Reactivity: | Human, Mouse |
Host Species: | Rabbit |
Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 1-100 of human PCYT1A (NP_001299602.1). |
Application: | WB |
Recommended Dilution: | WB 1:500 - 1:2000 |
Reactivity: | Human, Mouse |
Positive Samples: | HeLa, HepG2, Mouse testis, Mouse brain |
Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 1-100 of human PCYT1A (NP_001299602.1). |
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: | MDAQ CSAK VNAR KRRK EAPG PNGA TEED GVPS KVQR CAVG LRQP APFS DEIE VDFS KPYV RVTM EEAS RGTP CERP VRVY ADGI FDLF HSGH ARAL MQAK |
Gene ID: | 5130 |
Uniprot: | P49585 |
Cellular Location: | |
Calculated MW: | |
Observed MW: | 42kDa |
Synonyms: | PCYT1A, CCTA, CT, CTA, CTPCT, PCYT1, SMDCRD |
Background: | This gene belongs to the cytidylyltransferase family and is involved in the regulation of phosphatidylcholine biosynthesis. Mutations in this gene are associated with spondylometaphyseal dysplasia with cone-rod dystrophy. Alternatively spliced transcript variants have been found for this gene. |
UniProt Protein Function: | PCYT1A: Controls phosphatidylcholine synthesis. Homodimer. By phosphorylation. Belongs to the cytidylyltransferase family. |
UniProt Protein Details: | Protein type:Transferase; Lipid Metabolism - glycerophospholipid; EC 2.7.7.15 Chromosomal Location of Human Ortholog: 3q29 Cellular Component: endoplasmic reticulum membrane; glycogen granule Molecular Function:choline-phosphate cytidylyltransferase activity Biological Process: CDP-choline pathway; phosphatidylcholine biosynthetic process Disease: Spondylometaphyseal Dysplasia With Cone-rod Dystrophy |
NCBI Summary: | This gene belongs to the cytidylyltransferase family and is involved in the regulation of phosphatidylcholine biosynthesis. Mutations in this gene are associated with spondylometaphyseal dysplasia with cone-rod dystrophy. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2015] |
UniProt Code: | P49585 |
NCBI GenInfo Identifier: | 166214967 |
NCBI Gene ID: | 5130 |
NCBI Accession: | P49585.2 |
UniProt Secondary Accession: | P49585,Q86Y88, A9LYK9, D3DXB1, |
UniProt Related Accession: | P49585 |
Molecular Weight: | 41,731 Da |
NCBI Full Name: | Choline-phosphate cytidylyltransferase A |
NCBI Synonym Full Names: | phosphate cytidylyltransferase 1, choline, alpha |
NCBI Official Symbol: | PCYT1A |
NCBI Official Synonym Symbols: | CT; CTA; CCTA; CTPCT; PCYT1; SMDCRD |
NCBI Protein Information: | choline-phosphate cytidylyltransferase A |
UniProt Protein Name: | Choline-phosphate cytidylyltransferase A |
UniProt Synonym Protein Names: | CCT-alpha; CTP:phosphocholine cytidylyltransferase A; CCT A; CT A; Phosphorylcholine transferase A |
Protein Family: | Choline-phosphate cytidylyltransferase |
UniProt Gene Name: | PCYT1A |
UniProt Entry Name: | PCY1A_HUMAN |