Name : Galactosidase alpha Antibody
Supplier : BIOSS PRIMARY UNCONJUGATED ANTIBODIES
Price :263
SKU : GEN1254510102
| Long name | Galactosidase alpha Primary Polyclonal Antibody |
| Also known as | Galactosidase alpha PAb |
| Category | Primary Antibodies |
| Conjugation | Unconjugated |
| Target Antigen | Galactosidase alpha |
| Specificity | This is a highly specific antibody against Galactosidase alpha |
| Modification(s) | None |
| Modification site(s) | Unmodified antibody |
| Clonality | Polyclonal antibody |
| Clone number | Polyclonal antibody |
| Concentration | 1ug per 1ul |
| Immunogen range | 127-148/429 |
| Subcellular location | Lysosome |
| Source | This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human Galactosidase alpha |
| Gene ID number | 2717 |
| Swiss Prot | P06280 |
| 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 | Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk, Death results from renal failure, Defects in GLA are the cause of Fabry's disease (FD), FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues, Heterozygous females may exhibit the disorder in an attenuated form, Patients may show ocular deposits, and burning pain in the extremities, cardiac or cerebral complications of hypertension or other vascular disease, febrile episodes, galactomannans and galactohydrolase, including galactose oligosaccharides, non reducing alpha D galactose residues in alpha D galactosides, they are more likely to show corneal opacities, Galactosidase alpha is involved in the hydrolysis of terminal |
| 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 | Alpha-D-galactosidase A, Alpha-D-galactoside galactohydrolase, Alpha-galactosidase A, GLA, Melibiase, GALA |
| 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 | Galactosidase alpha |
| Short name | Galactosidase alpha Antibody |
| Technique | antibodies against human proteins, antibodies for, Antibody |
| Alternative name | Galactosidase a (Antibody to) |
| Alternative technique | antibodies |
| Identity | 4296 |
| Gene | GLA |
| Long gene name | galactosidase alpha |
| Synonyms | GALA |
| Locus | Xq22, 1 |
| Discovery year | 2001-06-22 |
| GenBank acession | X16889 |
| Entrez gene record | 2717 |
| Havana BLAST/BLAT | OTTHUMG00000022026 |
| Locus Specific Databases | Mental Retardation database LRG_672 |