Metabolism Antibodies 2
Anti-ADSL Antibody (CAB6278)
- SKU:
- CAB6278
- 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-ADSL Antibody |
Antibody SKU: | CAB6278 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IF IP |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-310 of human ADSL (NP_000017.1). |
Application: | WB IF IP |
Recommended Dilution: | WB 1:500 - 1:2000 IF 1:20 - 1:100 IP 1:50 - 1:100 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | HepG2, MCF7 |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-310 of human ADSL (NP_000017.1). |
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: | MAAG GDHG SPDS YRSP LASR YASP EMCF VFSD RYKF RTWR QLWL WLAE AEQT LGLP ITDE QIQE MKSN LENI DFKM AAEE EKRL RHDV MAHV HTFG HCCP KAAG IIHL GATS CYVG DNTD LIIL RNAL DLLL PKLA RVIS RLAD FAKE RASL PTLG FTHF QPAQ LTTV GKRC CLWI QDLC MDLQ NLKR VRDD LRFR GVKG TTGT QASF LQLF EGDD HKVE QLDK MVTE KAGF KRAF IITG QTYT RKVD IEVL SVLA SLGA SVHK ICTD IRLL ANLK EMEE PFEK QQIG SSAM PYKR NPMR SERC CSLA RH |
Gene ID: | 158 |
Uniprot: | P30566 |
Cellular Location: | |
Calculated MW: | 48kDa/54kDa |
Observed MW: | 55kDa |
Synonyms: | ADSL, AMPS, ASASE, ASL |
Background: | The protein encoded by this gene belongs to the lyase 1 family. It is an essential enzyme involved in purine metabolism, and catalyzes two non-sequential reactions in the de novo purine biosynthetic pathway: the conversion of succinylaminoimidazole carboxamide ribotide (SAICAR) to aminoimidazole carboxamide ribotide (AICAR) and the conversion of adenylosuccinate (S-AMP) to adenosine monophosphate (AMP). Mutations in this gene are associated with adenylosuccinase deficiency (ADSLD), a disorder marked with psychomotor retardation, epilepsy or autistic features. Alternatively spliced transcript variants have been found for this gene. |
UniProt Protein Function: | ADSL: Defects in ADSL are the cause of adenylosuccinase deficiency (ADSL deficiency). ADSL deficiency is an autosomal recessive disorder characterized by the accumulation in the body fluids of succinylaminoimidazole-carboxamide riboside (SAICA-riboside) and succinyladenosine (S-Ado). Most children display marked psychomotor delay, often accompanied by epilepsy or autistic features, or both, although some patients may be less profoundly retarded. Occasionally, growth retardation and muscular wasting are also present. Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily. 2 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:EC 4.3.2.2; Amino Acid Metabolism - alanine, aspartate and glutamate; Nucleotide Metabolism - purine; Lyase Chromosomal Location of Human Ortholog: 22q13.2 Cellular Component: cytosol Molecular Function:adenylosuccinate lyase activity Biological Process: AMP biosynthetic process; purine ribonucleoside monophosphate biosynthetic process; metabolic process; nucleobase, nucleoside and nucleotide metabolic process; purine nucleotide biosynthetic process; protein tetramerization; purine base metabolic process; 'de novo' IMP biosynthetic process Disease: Adenylosuccinase Deficiency |
NCBI Summary: | Adenylsuccinate lyase is involved in both de novo synthesis of purines and formation of adenosine monophosphate from inosine monophosphate. It catalyzes two reactions in AMP biosynthesis: the removal of a fumarate from succinylaminoimidazole carboxamide (SAICA) ribotide to give aminoimidazole carboxamide ribotide (AICA) and removal of fumarate from adenylosuccinate to give AMP. Adenylosuccinase deficiency results in succinylpurinemic autism, psychomotor retardation, and , in some cases, growth retardation associated with muscle wasting and epilepsy. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
UniProt Code: | P30566 |
NCBI GenInfo Identifier: | 6686318 |
NCBI Gene ID: | 158 |
NCBI Accession: | P30566.2 |
UniProt Secondary Accession: | P30566,O75495, Q5TI34, B0QY76, |
UniProt Related Accession: | P30566 |
Molecular Weight: | 484 |
NCBI Full Name: | Adenylosuccinate lyase |
NCBI Synonym Full Names: | adenylosuccinate lyase |
NCBI Official Symbol: | ADSL |
NCBI Official Synonym Symbols: | ASL; AMPS; ASASE |
NCBI Protein Information: | adenylosuccinate lyase; adenylosuccinase |
UniProt Protein Name: | Adenylosuccinate lyase |
UniProt Synonym Protein Names: | Adenylosuccinase; ASase |
Protein Family: | Adenylosuccinate lyase |
UniProt Gene Name: | ADSL |
UniProt Entry Name: | PUR8_HUMAN |
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