| Long name: |
ALEXA FLUOR 488 Conjugated, ALAD Polyclonal Antibody |
| Also known as: |
Anti-ALAD PAb ALEXA FLUOR 488 |
| Category: |
Conjugated Primary Antibodies |
| Conjugated with: |
488, ALEXA FLUOR® |
| Host Organism: |
Rabbit (Oryctolagus cuniculus) |
| Target Antigen: |
ALAD |
| Specificity: |
This is a highly specific antibody against ALAD |
| Modification: |
Unmodified |
| Modification Site: |
None |
| Clonality: |
Polyclonal |
| Clone: |
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) |
| Recommended dilutions: |
IF(IHC-P)(1:50-200) |
| Crossreactivity: |
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 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: |
Purified by Protein A |
| Storage conditions: |
50% glycerol and 0, Keep refrigerated at 2 to 8 degrees Celcius for up to one year, 09% sodium azide, Store this antibody in aqueous buffered solution containing 1% BSA |
| Excitation emission: |
499nm/519nm |
| Synonyms: |
ALADH PBGS |
| Properties: |
ALEXA FLUOR they should be stored frozen at - 24°, Alexa Fluor 488 has the same range to that of fluorescein isothiocyanate (FITC), Also Alexa Fluor 488 is pH stable, As a result of this photo stability, If you buy Antibodies supplied by Bioss Primary Conjugated Antibodies, It is distinguished in the FL1 of a FACS-Calibur or FACScan, has a very high photo stability, it has turned into an antibody for fluorescent microscopy and FACS FLOW cytometry, yet the ALAD Antibody, C, C for long term storage and for short term at + 5°, For facs or microscopy Alexa 1 conjugate |
| Conjugation: |
Alexa Fluor |
| Gene target: |
ALAD |
| Short name: |
ALAD Antibody |
| Technique: |
antibodies against human proteins, antibodies for, Antibody |
| Label: |
ALEXA FLUOR 488 |
| Alternative name: |
ALEXA FLUOR 488, 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 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 |