HEXB (NM_000521) Human 3' UTR Clone
CAT#: SC201097
3' UTR clone of hexosaminidase B (beta polypeptide) (HEXB) for miRNA target validation
Need custom modification / cloning service?
Get a free quote
CNY 4,845.00
货期*
3周
规格
Product images
经常一起买 (2)
Specifications
Product Data | |
Product Name | HEXB (NM_000521) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | ENC-1AS; HEL-248; HEL-S-111 |
ACCN | NM_000521 |
Insert Size | 143 bp |
Sequence Data |
>SC201097 3’UTR clone of NM_000521
The sequence shown below is from the reference sequence of NM_000521. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCTGGATATTGTAACCATGAGAACATGTAAAAAATGGAGGGGAAAAAGGCCACAGCAATCTGTACTACA ATCAACTTTATTTTGAAATCATGTAAAATAAGATATTAGACTGTTTTTTGAATAAAATATTTTTATTGA TTGAA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG |
Restriction Sites | SgfI-MluI |
OTI Disclaimer | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
Reference Data | |
RefSeq | NM_000521.4 |
Synonyms | ENC-1AS; HEL-248; HEL-S-111 |
Summary | Hexosaminidase B is the beta subunit of the lysosomal enzyme beta-hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Beta-hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes. Both beta-hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases. Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses. Beta subunit gene mutations lead to Sandhoff disease (GM2-gangliosidosis type II). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014] |
Locus ID | 3074 |
MW | 5.5 |
Documents
Product Manuals |
FAQs |
Resources
Customer
Reviews
Loading...