MNX1 (NM_005515) Human Untagged Clone

CAT#: SC303657

MNX1 (untagged)-Human motor neuron and pancreas homeobox 1 (MNX1), transcript variant 1



  "NM_005515" in other vectors (4)

CNY 5,488.00


货期*
现货

规格
    • 10 ug

Product images

经常一起买 (3)
Rabbit Polyclonal MNX1/HLXB9 Antibody
    • 100 ug

CNY 5,381.00


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

CNY 4,090.00


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 HB9; HLXB9; HOXHB9; SCRA1
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF sequence for NM_005515 edited
ATGGAAAAATCCAAAAATTTCCGCATCGACGCCCTGCTGGCGGTGGACCCCCCACGAGCC
GCCTCTGCGCAGAGCGCGCCGCTGGCCTTGGTCACGTCGCTCGCCGCCGCCGCATCTGGC
ACCGGAGGTGGCGGCGGCGGCGGCGGGGCGAGCGGCGGGACTAGCGGCAGCTGCAGCCCC
GCGTCCTCGGAGCCGCCGGCTGCGCCCGCCGACCGCCTGCGCGCCGAGAGCCCGTCGCCG
CCGCGCCTGCTGGCCGCGCACTGCGCGCTGCTGCCCAAGCCGGGCTTCCTGGGCGCGGGC
GGCGGCGGCGGCGGCACGGGCGGCGGGCACGGGGGGCCCCACCACCACGCGCATCCGGGC
GCAGCGGCCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCGCTGGGGGCCTGGCGCTGGGG
CTGCACCCTGGGGGCGCGCAGGGCGGCGCGGGCCTCCCGGCGCAGGCGGCGCTCTACGGC
CACCCGGTCTACGGCTACTCCGCGGCGGCGGCGGCGGCTGCGCTGGCGGGCCAGCACCCG
GCGCTCTCCTACTCGTACCCGCAGGTGCAAGGCGCGCACCCCGCGCACCCCGCCGACCCC
ATCAAGCTGGGCGCCGGCACCTTCCAGCTGGACCAGTGGCTGCGCGCGTCCACCGCGGGC
ATGATCCTGCCTAAGATGCCCGACTTCAACTCCCAGGCGCAGTCGAACCTCCTGGGGAAG
TGCCGCCGGCCGCGCACCGCCTTCACCAGCCAGCAGCTGCTGGAGCTGGAGCACCAGTTC
AAGCTCAACAAGTACCTGTCGCGGCCCAAGCGCTTCGAGGTGGCCACCTCGCTCATGCTC
ACCGAGACCCAGGTGAAGATTTGGTTCCAGAACCGGCGGATGAAATGGAAACGCAGCAAA
AAGGCCAAAGAGCAGGCGGCGCAGGAAGCGGAGAAACAGAAGGGCGGCGGCGGGGGCGCG
GGGAAGGGCGGCGCGGAGGAGCCGGGAGCCGAGGAGCTGCTGGGGCCGCCAGCGCCCGGA
GACAAGGGCAGCGGACGCCGCCTGCGGGACTTGAGGGACAGTGACCCCGAGGAGGACGAG
GACGAGGACGACGAGGACCATTTCCCCTACAGCAACGGCGCCAGCGTCCACGCCGCCTCC
TCCGACTGCTCCTCGGAGGACGACTCGCCGCCCCCGCGGCCCAGCCACCAGCCCGCGCCC
CAGTAG
Restriction Sites Please inquire     
ACCN NM_005515
Insert Size 1500 bp
OTI Disclaimer Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery.

The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
OTI Annotation It is not a varient.
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_005515.2, NP_005506.2
RefSeq Size 2061 bp
RefSeq ORF 1212 bp
Locus ID 3110
UniProt ID P50219
Protein Families Druggable Genome, ES Cell Differentiation/IPS
Protein Pathways Maturity onset diabetes of the young
Gene Summary This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
Transcript Variant: This variant (1) encodes the longer 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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