Acid Phosphatase 2 (ACP2) (NM_001131064) Human 3' UTR Clone

Specifications

Product Data
Product Name	Acid Phosphatase 2 (ACP2) (NM_001131064) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	acid phosphatase 2, lysosomal; Acp-2; LAP; OTTMUSP00000015308
ACCN	NM_001131064
Insert Size	160 bp
Sequence Data	Insert Sequence (showhide) >SC201066 3’UTR clone of NM_001131064 The sequence shown below is from the reference sequence of NM_001131064. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGAGTGGCCAGCCCTTCCCTGGGGTGGTGAGGGGACAGCTCTGGCCGTAGGCCTGCTGATGCCAGGCTC CTTTTCCCGCTGCCTGTTTCCCCGCTTCGCTCTACAGCTGCTGAAGTTCCCGTTGGGCCCATGTCCCCG TTATGAGCAGCTGCAGAACGAG 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_001131064.1
Synonyms	acid phosphatase 2, lysosomal; Acp-2; LAP; OTTMUSP00000015308
Summary	The protein encoded by this gene belongs to the histidine acid phosphatase family, which hydrolyze orthophosphoric monoesters to alcohol and phosphate. This protein is localized to the lysosomal membrane, and is chemically and genetically distinct from the red cell acid phosphatase. Mice lacking this gene showed multiple defects, including bone structure alterations, lysosomal storage defects, and an increased tendency towards seizures. An enzymatically-inactive allele of this gene in mice showed severe growth retardation, hair-follicle abnormalities, and an ataxia-like phenotype. Alternatively spliced transcript variants have been found for this gene. A C-terminally extended isoform is also predicted to be produced by the use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism. [provided by RefSeq, Oct 2017]
Locus ID	53
MW	5.5

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