| Long name: |
ALAD Primary Polyclonal Antibody |
| Also known as: |
ALAD PAb |
| Category: |
Primary Antibodies |
| Conjugation: |
Unconjugated |
| Target Antigen: |
ALAD |
| Specificity: |
This is a highly specific antibody against ALAD |
| Modification(s): |
None |
| Modification site(s): |
Unmodified antibody |
| Clonality: |
Polyclonal antibody |
| Clone number: |
Polyclonal antibody |
| Concentration: |
1ug per 1ul |
| Source: |
This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human ALAD |
| Gene ID number: |
210 |
| Tested Applications: |
IF(IHC-P), IHC-P, WB |
| Recommended dilutions: |
IF(IHC-P)(1:50-200), IHC-P(1:100-500), WB(1:100-1000) |
| Cross reactivity: |
Mouse, Rat, Human |
| Cross reactive species details: |
not every possible cross-reactivity is known, Due to limited amount of testing and knowledge |
| Background of the target antigen: |
AHP is a form of porphyria, AHP is characterized by attacks of gastrointestinal disturbances, Binds two molecules of 5-aminolevulinate per subunit, Most attacks are precipitated by drugs, Porphyrias are inherited defects in the biosynthesis of heme, They are classified as erythropoietic or hepatic, abdominal colic, alcohol, and catalyzes their condensation to form porphobilinogen, and peripheral neuropathy, caloric deprivation, depending on whether the enzyme deficiency occurs in red blood cells or in the liver, each at a distinct site, infections, or endocrine factors, paralysis, resulting in the accumulation and increased excretion of porphyrins or porphyrin precursors, Catalyzes an early step in the biosynthesis of tetrapyrroles, Involvement in disease:Defects in ALAD are the cause of acute hepatic porphyria (AHP) |
| Purification method: |
This antibody was purified via Protein A |
| Storage conditions: |
50% glycerol and 0, Store at -20°, 09% sodium azide, C for up to 1 year, Keep the antibody in aqueous buffered solution containing 1% BSA |
| Synonym names: |
ALADH, ALADR, Aminolevulinate, Aminolevulinate dehydratase, Delta aminolevulinic acid dehydratase, Delta-aminolevulinic acid dehydratase, HEM2_HUMAN, Lv, PBGS, Porphobilinogen synthase, dehydratase, delta, ALAD |
| Properties: |
C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by Bioss Primary Unconjugated Antibodies they should be stored frozen at - 24° |
| Gene target: |
ALAD |
| Short name: |
ALAD Antibody |
| Technique: |
antibodies against human proteins, antibodies for, Antibody |
| Alternative name: |
ALAD (Antibody to) |
| Alternative technique: |
antibodies |
| Identity: |
395 |
| Gene: |
ALAD |
More about : ALAD |
| Long gene name: |
aminolevulinate dehydratase |
| Synonyms gene name: |
aminolevulinate, dehydratase , delta- |
| Synonyms: |
ALADH PBGS |
| Synonyms name: |
porphobilinogen synthase |
| Locus: |
9q32 |
| Discovery year: |
1986-01-01 |
| GenBank acession: |
M13928 |
| Entrez gene record: |
210 |
| Pubmed identfication: |
6839527 6378062 |
| RefSeq identity: |
NM_001003945 |
| Havana BLAST/BLAT: |
OTTHUMG00000020522 |
| Locus Specific Databases: |
ALSOD, the Amyotrophic Lateral Sclerosis Online Genetic Database |