Metabolism Antibodies 1
Anti-ALDOA Antibody (CAB1142)
- SKU:
- CAB1142
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Metabolism
Description
Antibody Name: | Anti-ALDOA Antibody |
Antibody SKU: | CAB1142 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IF |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-348 of human ALDOA (NP_908930.1). |
Application: | WB IF |
Recommended Dilution: | WB 1:500 - 1:2000 IF 1:20 - 1:100 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | MCF7, DU145, 293T, HepG2, Jurkat, A-549, CEM, Mouse skeletal muscle, Mouse kidney |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-348 of human ALDOA (NP_908930.1). |
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: | MPYQ YPAL TPEQ KKEL SDIA HRIV APGK GILA ADES TGSI AKRL QSIG TENT EENR RFYR QLLL TADD RVNP CIGG VILF HETL YQKA DDGR PFPQ VIKS KGGV VGIK VDKG VVPL AGTN GETT TQGL DGLS ERCA QYKK DGAD FAKW RCVL KIGE HTPS ALAI MENA NVLA RYAS ICQQ NGIV PIVE PEIL PDGD HDLK RCQY VTEK VLAA VYKA LSDH HIYL EGTL LKPN MVTP GHAC TQKF SHEE IAMA TVTA LRRT VPPA VTGI TFLS GGQS EEEA SINL NAIN KCPL LKPW ALTF SYGR ALQA SALK AWGG KKEN LKAA QEEY VKRA LANS LACQ GKYT PSGQ |
Gene ID: | 226 |
Uniprot: | P04075 |
Cellular Location: | Cytoplasm, I band, M line, myofibril, sarcomere |
Calculated MW: | 39kDa/45kDa |
Observed MW: | 43kDa |
Synonyms: | ALDOA, ALDA, GSD12, HEL-S-87p |
Background: | The protein encoded by this gene, Aldolase A (fructose-bisphosphate aldolase), is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1, 6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing and alternative promoter usage results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 3 and 10. |
UniProt Protein Function: | ALDOA: a glycolytic enzyme that catalyzes D-fructose 1,6-bisphosphate -> glycerone phosphate + D-glyceraldehyde 3-phosphate. Three forms of aldolase are found in vertebrates - aldolase A in muscle, aldolase B in liver and aldolase C in brain. |
UniProt Protein Details: | Protein type:Carbohydrate Metabolism - glycolysis and gluconeogenesis; EC 4.1.2.13; Carbohydrate Metabolism - fructose and mannose; Lyase; Carbohydrate Metabolism - pentose phosphate pathway; Mitochondrial Chromosomal Location of Human Ortholog: 16p11.2 Cellular Component: I band; extracellular space; membrane; extracellular region; M band; cytosol; nucleus; actin cytoskeleton Molecular Function:tubulin binding; identical protein binding; protein binding; cytoskeletal protein binding; fructose-bisphosphate aldolase activity; actin binding Biological Process: platelet activation; striated muscle contraction; glycolysis; glucose metabolic process; actin filament organization; pathogenesis; protein homotetramerization; gluconeogenesis; muscle maintenance; regulation of cell shape; fructose 1,6-bisphosphate metabolic process; platelet degranulation; ATP biosynthetic process; carbohydrate metabolic process; blood coagulation; fructose metabolic process Disease: Glycogen Storage Disease Xii |
NCBI Summary: | The protein encoded by this gene, Aldolase A (fructose-bisphosphate aldolase), is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing and alternative promoter usage results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 3 and 10. [provided by RefSeq, Aug 2011] |
UniProt Code: | P04075 |
NCBI GenInfo Identifier: | 113606 |
NCBI Gene ID: | 226 |
NCBI Accession: | P04075.2 |
UniProt Secondary Accession: | P04075,Q6FH76, Q6FI10, Q96B15, Q9BWD9, Q9UCN2, B4DXI7 |
UniProt Related Accession: | P04075 |
Molecular Weight: | 364 |
NCBI Full Name: | Fructose-bisphosphate aldolase A |
NCBI Synonym Full Names: | aldolase A, fructose-bisphosphate |
NCBI Official Symbol: | ALDOA |
NCBI Official Synonym Symbols: | ALDA; GSD12; HEL-S-87p |
NCBI Protein Information: | fructose-bisphosphate aldolase A; muscle-type aldolase; lung cancer antigen NY-LU-1; fructose-1,6-bisphosphate triosephosphate-lyase; epididymis secretory sperm binding protein Li 87p |
UniProt Protein Name: | Fructose-bisphosphate aldolase A |
UniProt Synonym Protein Names: | Lung cancer antigen NY-LU-1; Muscle-type aldolase |
Protein Family: | Fructose-bisphosphate aldolase |
UniProt Gene Name: | ALDOA |
UniProt Entry Name: | ALDOA_HUMAN |