Description : |
Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targeted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. |
Source : |
HEK293 |
Species : |
Human |
Tag : |
Myc/DDK |
Molecular Mass : |
59.69 kDa |
AA Sequence : |
MGPRGAASLPRGPGPRRLLLPVVLP LLLLLLLAPPGSGAGASRPPHLVFL LADDLGWNDVGFHGSRIRTPHLDAL AAGGVLLDNYYTQPLCTPSRSQLLT GRYQIRTGLQHQIIWPCQPSCVPLD EKLLPQLLKEAGYTTHMVGKWHLGM YRKECLPTRRGFDTYFGYLLGSEDY YSHERCTLIDALNVTRCALDFRDGE EVATGYKNMYSTNIFTKRAIALITN HPPEKPLFLYLALQSVHEPLQVPEE YLKPYDFIQDKNRHHYAGMVSLMDE AVGNVTAALKSSGLWNNTVFIFSTD NGGQTLAGGNNWPLRGRKWSLWEGG VRGVGFVASPLLKQKGVKNRELIHI SDWLPTLVKLARGHTNGTKPLDGFD VWKTISEGSPSPRIELLHNIDPNFV DSSPCPRNSMAPAKDDSSLPEYSAF NTSVHAAIRHGNWKLLTGYPGCGYW FPPPSQYNVSEIPSSDPPTKTLWLF DIDRDPEERHDLSREYPHIVTKLLS RLQFYHKHSVPVYFPAQDPRCDPKA TGVWGPWMTRTRPLEQKLISEEDLA ANDILDYKDDDDKV |
Purity : |
> 80% as determined by SDS-PAGE and Coomassie blue staining |
Stability : |
Stable for 3 months from receipt of products under proper storage and handling conditions. |
Storage : |
Store at -80 centigrade. Avoid repeated freeze-thaw cycles. |
Concentration : |
50 μg/mL as determined by BCA |
Storage Buffer : |
100 mM glycine, 25 mM Tris-HCl, pH 7.3. |