DFNB31 (WHRN) (NM_001083885) Human Untagged Clone

CAT#: SC316062

DFNB31 (untagged)-Human deafness, autosomal recessive 31 (DFNB31), transcript variant 2



  "NM_001083885" in other vectors (4)

CNY 7,220.00


货期*
5周

规格
    • 10 ug

Product images

经常一起买 (4)
WHRN Rabbit polyclonal Antibody
    • 100 ul

CNY 1,999.00
CNY 3,280.00


TurboFectin Transfection Reagent (1 mL in 1 vial)
    • 1 ml in 1 vial

CNY 4,090.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00


Forward sequencing primer VP1.5, Reverse sequencing primer XL39, 100pmoles each
    • 100 pmol

CNY 480.00

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.
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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