ARSD polyclonal, anti-human, mouse
€305.00
In stock
SKU
BS60837
Background:
Arylsulfatase D, also known as ARSD, is a 593 amino acid protein that localizes to the lysosome and belongs to the sulfatase family of bone and cartilage matrix proteins. Existing as three alternatively spliced isoforms which are expressed in liver, pancreas, kidney, heart, brain, lung and placenta, Arylsulfatase D uses calcium as a cofactor to catalyze reactions that are important in maintaining correct bone composition. The gene encoding Arylsulfatase D maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.
Alternative Name:
Arylsulfatase D, ASD, ARSD
Application Dilution: WB: 1:500~1:1000
Specificity: ARSD polyclonal antibody detects endogenous levels of ARSD protein.
Immunogen:
A synthetic peptide corresponding to residues in Human ARSD.
MW: ~ 42 kDa
Swis Prot.: P51689
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1 mg/ml in Phosphate buffered saline (PBS) with 15 mM sodium azide, approx. pH 7.2.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
Arylsulfatase D, also known as ARSD, is a 593 amino acid protein that localizes to the lysosome and belongs to the sulfatase family of bone and cartilage matrix proteins. Existing as three alternatively spliced isoforms which are expressed in liver, pancreas, kidney, heart, brain, lung and placenta, Arylsulfatase D uses calcium as a cofactor to catalyze reactions that are important in maintaining correct bone composition. The gene encoding Arylsulfatase D maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.
Alternative Name:
Arylsulfatase D, ASD, ARSD
Application Dilution: WB: 1:500~1:1000
Specificity: ARSD polyclonal antibody detects endogenous levels of ARSD protein.
Immunogen:
A synthetic peptide corresponding to residues in Human ARSD.
MW: ~ 42 kDa
Swis Prot.: P51689
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1 mg/ml in Phosphate buffered saline (PBS) with 15 mM sodium azide, approx. pH 7.2.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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