HPS2 (AP3B1) (NM_003664) Human 3' UTR Clone

Specifications

Product Data
Product Name	HPS2 (AP3B1) (NM_003664) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	ADTB3; ADTB3A; HPS; HPS2; PE
ACCN	NM_003664
Insert Size	606 bp
Sequence Data	Insert Sequence (showhide) >SC207933 3’UTR clone of NM_003664 The sequence shown below is from the reference sequence of NM_003664. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAACTGAAGCCTGTCCTGTCTCAGGGGTAACCTGCTTACATCTGGACTTTAGAATCTGGCACACAACAA AAGTGCCTGGCATCCACTACTGCTGCCTTTCATTTATAATAATAGCCCTTCCATCTGGCAGTGGGGGTA GAATACACTCTTGACATTCTTGTCTCCTGCTTTAGAATGCTAGTGTGTATCTATCATGTATGCAATACT TTCCCCCTTTTTGCTTTGCTAACCAAAGAGCATATATTTTACTGTCAGTTGTCTCAACTCTTGAATCCA TGTGGCGTTTTCTCTGTCCTGCTGCTTCTTTTGGCCTCCTCGTTTTCCTTCTCTTTTTCGACAATGGTA GACATGAATGAGATATTTAAAGTTCATTGGAAATCTTCTTCCCTACAGCAGTAAGCAAAAATTAGCAAA GAGATAGTCTAAATGGCCTCTCAGCTTGGTATGTGAAAATGAGATCACATACTTTTTAAATCCAAATAC AAAAGCATAGTCTCTGCAAGATTTTGTTCTTTGAATTTCTTGATATTGTAATTGATTATTGATAACTGT CATCATGAAATTATCTCTCAATAATAAGATAAATAAACTAGCATATGAATCATA 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_003664.5
Synonyms	ADTB3; ADTB3A; HPS; HPS2; PE
Summary	This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. The encoded protein is part of the heterotetrameric AP-3 protein complex which interacts with the scaffolding protein clathrin. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2012]
Locus ID	8546
MW	22.9

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