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Home TrueClone ATP2C1 Clone

ATP2C1 (NM_001001485) Human cDNA Clone

Specifications Citations Clones of Other Species Product Documents
SKU Description Price Availibility*  
SC300199 ATP2C1 (untagged)-Human ATPase, Ca++ transporting, type 2C, member 1 (ATP2C1), transcript variant 3 (10ug), NM_001001485.1, 10ug $680 5 weeks
TF81001 TurboFectin, High performance Transfection reagent (1ml/vial) $420 In Stock
TA319887 Rabbit Polyclonal ATP2C1 Antibody, 100ug $325 3-7 Days
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OriGene Data
Vector:pCMV6-XL Insert Size: Restriction Site:
Sequence Data: Fully Sequenced ORF          5' Read Nucleotide Sequence         
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
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).
Product Components: The cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
Protein Families: TransmembraneDruggable Genome
Reference Data
RefSeq: NM_001001485.1, NP_001001485
RefSeq Size: 3389 RefSeq ORF: 2667
Synonyms : ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1
LocusID: 27032 Cytogenetic: 3q22.1
Summary: The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011].

Transcript Variant: This variant (3) has an alternate 5' sequence and lacks an internal exon in the 3' region, as compared to variant 6. The resulting isoform (1c) has shorter and distinct N- and C-termini, as compared to isoform 2a. Variants 3 and 11 encode the same isoform 1c.

* Delivery time is an estimate in business days. Occasional delays may occur due to unforeseen complexities in the preparation of your construct. International customers may expect an additional 1-2 weeks in shipping

 

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