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DFNB31 (WHRN) (NM_001083885) Human Untagged Clone
CAT＃: SC316062
DFNB31 (untagged)-Human deafness, autosomal recessive 31 (DFNB31), transcript variant 2
CNY 7,220.00
Product images
Specifications
| Product Data | |
| Type | Human Untagged Clone |
| Tag | Tag Free |
| Synonyms | CIP98; DFNB31; PDZD7B; USH2D; WI |
| Vector | pCMV6 series |
| Sequence Data |
>NCBI ORF sequence for NM_001083885, the custom clone sequence may differ by one or more nucleotides
ATGGCGAACTCGGCAGGGTTTCTTGGCGATCTCACAACAGAAGGAATAAACAAGCCAGGA TTTTACAAGGGCCCAGCCGGCTCCCAGGTGACCCTGAGCAGCCTGGGGAACCAGACACGA GTGCTGCTGGAGGAGCAGGCTCGGCACCTGCTGAACGAGCAGGAACACGCCACCATGGCC TACTACCTGGATGAGTACCGTGGTGGCAGCGTCTCTGTGGAGGCCCTCGTCATGGCCCTG TTCAAGCTGCTCAACACCCACGCCAAGTTCTCACTCCTCTCTGAGGTGAGAGGCACCATT TCCCCGCAAGACCTAGAACGCTTCGACCACCTGGTGCTGAGGCGTGAGATTGAGTCCATG AAGGCGCGGCAGCCCCCAGGCCCCGGGGCTGGGGACACCTACTCCATGGTCTCCTACAGT GACACGGGTTCATCCACAGGCAGCCACGGCACCTCCACCACCGTCAGCTCGGCCAGGAAC ACTCTGGACCTGGAGGAAACTGGCGAGGCTGTCCAGGGCAATATCAACGCCCTCCCAGAT GTGTCCGTGGATGATGTCAGATCCACCTCCCAGGGGCTGTCAAGCTTCAAGCCACTGCCT CGCCCACCACCTCTGGCCCAAGGCAACGACCTCCCACTAGGCCAGCCAAGGAAGCTGGGG AGAGAGGACCTCCAGCCACCTTCCTCCATGCCTTCCTGCTCGGGCACTGTCTTCTCGGCT CCACAGAACCGCAGCCCGCCAGCGGGCACCGCACCCACCCCAGGGACCTCCTCTGCACAG GACTTGCCCTCTTCCCCCATCTATGCCTCCGTCTCCCCTGCCAACCCCAGCTCCAAGAGG CCGCTGGACGCCCATCTGGCCCTGGTCAACCAACACCCCATCGGCCCCTTCCCACGGGTC CAGTCACCCCCGCACCTGAAAAGCCCCTCTGCAGAGGCCACAGTGGCTGGGGGCTGCCTT CTGCCCCCATCACCCTCTGGCCACCCAGACCAGACAGGCACAAACCAGCACTTTGTCATG GTGGAGGTCCACCGCCCCGACAGCGAGCCAGACGTCAATGAAGTGAGGGCGCTGCCCCAG ACGCGCACAGCCTCTACGCTCTCCCACCTCTCGGACAGCGGGCAGACTCTAAGCGAGGAC AGTGGTGTGGATGCTGGCGAGGCAGAGGCCAGCGCCCCAGGCCGAGGAAGGCAGTCGGTG TCCACCAAGAGCAGGAGTAGCAAGGAGCTGCCTCGGAACGAGAGGCCCACAGATGGGGCC AACAAACCGCCTGGACTTCTGGAGCCCACGTCCACTCTGGTCCGTGTGAAGAAAAGTGCG GCCACCCTGGGCATCGCCATCGAGGGTGGCGCCAACACCCGCCAGCCCCTGCCTAGGATT GTCACTATTCAGAGAGGCGGCTCAGCTCACAACTGTGGGCAGCTCAAGGTGGGCCACGTG ATTCTGGAAGTGAATGGGCTGACGCTTCGGGGCAAGGAGCACCGGGAGGCCGCCCGCATT ATCGCCGAGGCCTTCAAGACTAAGGACCGTGACTACATTGACTTTCTGGTCACTGAGTTC AATGTGATGCTC |
| Restriction Sites | Please inquire |
| ACCN | NM_001083885 |
| OTI Disclaimer | Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP). |
| OTI Annotation | This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA. |
| Product Components | The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water). |
| Reconstitution | 1. Centrifuge at 5,000xg for 5min. 2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA. 3. Close the tube and incubate for 10 minutes at room temperature. 4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom. 5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C. |
| Note | Plasmids are not sterile. For experiments where strict sterility is required, filtration with 0.22um filter is required. |
| Reference Data | |
| RefSeq | NM_001083885.1, NP_001077354.1 |
| RefSeq Size | 2944 bp |
| RefSeq ORF | 1575 bp |
| Locus ID | 25861 |
| UniProt ID | Q9P202 |
| Gene Summary | This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016] Transcript Variant: This variant (2) has multiple differences in the presence and absence of exons at its 5' end, compared to variant 1. These differences produce a unique 5' UTR and cause translation initiation at a downstream start codon, compared to variant 1. The encoded protein (isoform 2) is shorter than isoform 1. |
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
Other Versions
| SKU | Description | Size | Price |
|---|---|---|---|
| RC213282 | DFNB31 (Myc-DDK-tagged)-Human deafness, autosomal recessive 31 (DFNB31), transcript variant 2 |
CNY 4,560.00 |
|
| RC213282L3 | Lenti-ORF clone of DFNB31 (Myc-DDK-tagged)-Human deafness, autosomal recessive 31 (DFNB31), transcript variant 2 |
CNY 6,460.00 |
|
| RC213282L4 | Lenti-ORF clone of DFNB31 (mGFP-tagged)-Human deafness, autosomal recessive 31 (DFNB31), transcript variant 2 |
CNY 6,460.00 |
|
| RG213282 | DFNB31 (tGFP-tagged) - Human deafness, autosomal recessive 31 (DFNB31), transcript variant 2 |
CNY 5,040.00 |
