Product Name
ATP6V0A2, cDNA Clone
Full Product Name
ATP6V0A2 cDNA Clone
Product Gene Name
ATP6V0A2 cdna clone
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Sequence
atggggtccc tgttccggag cgagaccatg tgcctggcgc agctcttcct gcagtcgggc acggcctacg agtgcctcag cgccctgggc gagaaaggcc tggtccagtt ccgagacctc aaccagaacg taagttcttt ccaaagaaaa tttgttggtg aggtgaagag gtgtgaagag ctagagcgaa tattggtgta tttggtacag gaaattaata gagctgatat tccccttcct gaaggagagg ccagccctcc tgcgccaccc ctgaaacagg ttctagaaat gcaggagcag ttgcagaagc tcgaggttga actgagagaa gtcactaaga acaaggagaa actgaggaaa aacttgctgg aactgataga gtacactcac atgctgagag tgacaaagac ctttgtgaaa cgcaacgttg agtttgaacc cacttatgaa gaattccctt ccttagagag cgattctttg ttggattaca gctgtatgca gaggctggga gcaaaactgg gatttgtgtc tggcctaatt aaccaaggaa aagtggaagc atttgaaaaa atgttgtgga gagtctgcaa agggtacacc atcgtgtcct atgcagaact ggatgaatcc cttgaagacc ctgaaacagg ggaagtcata aaatggtatg tctttttaat atccttttgg ggagagcaga ttggccacaa ggttaagaag atatgtgatt gctaccactg ccacgtgtac ccctatccaa acacagccga ggagcggagg gagatccagg aggggctgaa cacccgcatc caggatctct acactgtact gcacaaaacc gaggactatt tgaggcaagt gctatgtaaa gccgccgagt ctgtctacag ccgtgtgatc caggtgaaga aaatgaaggc catctatcac atgctgaaca tgtgcagctt tgacgtgacc aacaagtgcc tcattgctga ggtctggtgt cccgaggcgg atctgcagga cctgcgccgg gcactggagg agggctcgag agagagtggt gctacaatcc cctcattcat gaatataatc cccacaaaag aaacaccccc cactcggatc cgcaccaaca aattcaccga gggatttcag aacatcgtgg atgcttatgg agtcggaagc tacagagaag tcaatccagc tctctttacc atcatcacct tcccgttttt atttgctgtg atgtttggag acttcggaca tggctttgtg atgtttttat ttgccctctt gttggtgtta aatgaaaatc atcccagact aaatcagtca caagagatca tgaggatgtt ttttaatggc cggtacatcc tcctgctgat ggggctgttc tcagtgtaca ctggcctcat ctacaacgac tgcttttcaa agtcagtcaa cctgttcggc tctgggtgga acgtgtcggc catgtacagc tccagccacc cacccgcaga gcataagaag atggtgcttt ggaacgacag cgtcgttaga cacaacagca ttttgcagct ggatccaagc attcctggag tgttccgagg cccttatccc cttggcattg atcctatttg gaacttggcc acaaatcgcc tcacttttct aaactctttc aaaatgaaaa tgtccgtgat tttaggaatc attcatatga cttttggagt cattctggga atatttaacc acttgcactt caggaagaag ttcaacattt acctggtttc catcccggaa cttctcttca tgctctgtat ctttggatac cttatattta tgattttcta caagtggctg gttttttcag cagaaacctc cagagttgct cccagcattc tgattgaatt tattaacatg tttttattcc cagccagtaa aacaagtggc ctttacacag ggcaggagta tgtccagaga gtgctgctgg ttgtcacagc attgtctgtc cctgtcctct tcttgggaaa gccactgttt ttgttgtggc ttcacaatgg gcgtagttgc ttcggggtga accggagtgg ctacacactt ataaggaaag atagtgagga agaagtttca ttgctgggaa gccaagatat agaagaggga aatcaccagg tggaagatgg atgtagagaa atggcgtgtg aagagtttaa ttttggagaa atattaatga cccaagtaat ccattccatc gagtactgtc tgggatgcat ctccaacacc gcctcctacc tgaggctctg ggcgcttagc ctggctcacg cacagttgtc tgatgtcctg tgggccatgc tgatgcgcgt gggcctccgc gttgacacca cctatggcgt cttgctactg ctcccggtta tcgcgctctt tgcagttttg accattttca tccttctgat catggaaggg ctttctgcgt ttcttcacgc catacgcctc cactgggtag aatttcagaa caaattctac gttggtgcag gcaccaaatt tgttcctttc tcattcagtc tactttcatc aaagttcaat aacgacgaca gtgtggcatg a
Clone Sequence Report
Provided with product shipment
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of ATP6V0A2 cdna clone vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
NCBI/Uniprot data below describe general gene information for ATP6V0A2. It may not necessarily be applicable to this product.
NCBI Accession #
BC068531
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UniProt Secondary Accession #
Q6NUM0; A8K026[Other Products]
UniProt Related Accession #
Q9Y487[Other Products]
Molecular Weight
98,082 Da
NCBI Official Full Name
Homo sapiens ATPase, H+ transporting, lysosomal V0 subunit a2, mRNA
NCBI Official Synonym Full Names
ATPase H+ transporting V0 subunit a2
NCBI Official Symbol
ATP6V0A2??[Similar Products]
NCBI Official Synonym Symbols
A2; RTF; TJ6; WSS; ARCL; J6B7; STV1; TJ6M; TJ6S; VPH1; ARCL2A; ATP6A2; ATP6N1D
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NCBI Protein Information
V-type proton ATPase 116 kDa subunit a isoform 2
UniProt Protein Name
V-type proton ATPase 116 kDa subunit a isoform 2
UniProt Synonym Protein Names
Lysosomal H(+)-transporting ATPase V0 subunit a2; TJ6; Vacuolar proton translocating ATPase 116 kDa subunit a isoform 2
Protein Family
V-type proton ATPase
UniProt Gene Name
ATP6V0A2??[Similar Products]
UniProt Synonym Gene Names
V-ATPase 116 kDa isoform a2??[Similar Products]
UniProt Entry Name
VPP2_HUMAN
NCBI Summary for ATP6V0A2
The protein encoded by this gene is a subunit of the vacuolar ATPase (v-ATPase), an heteromultimeric enzyme that is present in intracellular vesicles and in the plasma membrane of specialized cells, and which is essential for the acidification of diverse cellular components. V-ATPase is comprised of a membrane peripheral V(1) domain for ATP hydrolysis, and an integral membrane V(0) domain for proton translocation. The subunit encoded by this gene is a component of the V(0) domain. Mutations in this gene are a cause of both cutis laxa type II and wrinkly skin syndrome. [provided by RefSeq, Jul 2009]
UniProt Comments for ATP6V0A2
ATP6V0A2: Part of the proton channel of V-ATPases. Essential component of the endosomal pH-sensing machinery. May play a role in maintaining the Golgi functions, such as glycosylation maturation, by controlling the Golgi pH. Defects in ATP6V0A2 are the cause of cutis laxa autosomal recessive type 2A (ARCL2A). An autosomal recessive disorder characterized by an excessive congenital skin wrinkling, a large fontanelle with delayed closure, a typical facial appearance with downslanting palpebral fissures, a general connective tissue weakness, and varying degrees of growth and developmental delay and neurological abnormalities. Some affected individuals develop seizures and mental deterioration later in life, whereas the skin phenotype tends to become milder with age. At the molecular level, an abnormal glycosylation of serum proteins is observed in many cases. Defects in ATP6V0A2 are a cause of wrinkly skin syndrome (WSS). WSS is rare autosomal recessive disorder characterized by wrinkling of the skin of the dorsum of the hands and feet, an increased number of palmar and plantar creases, wrinkled abdominal skin, multiple musculoskeletal abnormalities, microcephaly, growth failure and developmental delay. Belongs to the V-ATPase 116 kDa subunit family.
Protein type: Transporter, ion channel; Membrane protein, integral; Transporter, iron; Membrane protein, multi-pass; Energy Metabolism - oxidative phosphorylation; Transporter
Chromosomal Location of Human Ortholog: 12q24.31
Cellular Component: cytoplasm; endosome membrane; focal adhesion; lysosomal membrane; phagocytic vesicle membrane; plasma membrane; vacuolar proton-transporting V-type ATPase complex
Molecular Function: ATPase binding; hydrogen ion transporting ATPase activity, rotational mechanism; protein binding
Biological Process: ATP synthesis coupled proton transport; immune response; insulin receptor signaling pathway; transferrin transport; vacuolar acidification
Disease: Cutis Laxa, Autosomal Recessive, Type Iia; Wrinkly Skin Syndrome
Research Articles on ATP6V0A2
1. the results from this study demonstrate that the a2-subunit isoform of Vacuolar ATPase regulates Notch signaling in breast tumor cells
Precautions
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Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.
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