The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Dec 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ARSABA-20-REGO | 20 (40 μL) | 200 μL |
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| ARSABA-20-REGR | 20 (40 μL) | 200 μL |
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| ARSABA-20-ORGR | 20 (40 μL) | 200 μL |
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| ARSABA-20-GOGR | 20 (40 μL) | 200 μL |
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| ARSABA-20-GRRE | 20 (40 μL) | 200 μL |
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| ARSABA-20-GROR | 20 (40 μL) | 200 μL |
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| ARSABA-20-GRGO | 20 (40 μL) | 200 μL |
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| ARSABA-20-AQOR | 20 (40 μL) | 200 μL |
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The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Dec 2010]
Gene Symbol : ARSA
Gene Name : Arylsulfatase A
Chromosome : CHR 22: 506,281,72-506,227,53
Locus : 22q13.33
Alt. Genes : CLEC3A
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