ACYP2 (NM_138448) Human Untagged Clone

CAT#: SC324123

ACYP2 (untagged)-Human acylphosphatase 2, muscle type (ACYP2)



  "NM_138448" in other vectors (5)

CNY 1,200.00

CNY 3,990.00


货期*
现货

规格
    • 10 ug

Product images

经常一起买 (3)
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 ACYM; ACYP
Vector pCMV6-AC
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
>OriGene sequence for NM_138448.2 CGGCTGCCCTCGCTCCCAGGCCCCGCAGTCTCATTTGCCGCTTCCGACGCGTGACCCCGG
CGCGCTAGCGTCCGGGACCGGTGACAGGCGCGGGGTGCGCCAAGCAGTCCCATGTGTCCC
CTCCCTCTCGCAGCCGCCGCAGTCGCTGCGCCCCGAGCCCCTCTCCGGCTCCTCAACAGA
GGGCTCGCCGCCGCCATGTCTACCGCCCAGTCACTCAAATCCGTGGACTACGAGGTGTTC
GGAAGAGTGCAGGGTGTTTGCTTCAGAATGTATACAGAAGATGAAGCTAGGAAAATAGGA
GTGGTTGGCTGGGTGAAGAATACCAGCAAAGGCACCGTGACAGGCCAAGTGCAGGGGCCA
GAAGACAAAGTCAATTCCATGAAGTCCTGGCTGAGCAAGGTTGGAAGCCCTAGTTCTCGC
ATTGACCGCACAAACTTTTCTAATGAAAAAACCATCTCTAAGCTTGAATACTCTAATTTT
AGTATTAGATACTAATAGAAGAGAAAAATTGTAACACACTGAACAATAGATACTGTATGT
TCTTAAGACTATGTATACTAGAATAATAGTAGCAGAGTAGGGTGAAAAGGAACTTTCTGT
TCTGAAAGCTAAGCGACTGTACGTGCTACTAAAAATGTCTGACACTGAAATAATTTTACT
CAACTATGTTTTCAACAAGCAAAAATATAGTATTCTAAGATTAAAATGTCATTACAAAAT
ATTTAGTGTGAACATTTAATTTAAACTTGTCTCATGGAATCTTTAATTTCAATGAACATT
ACAGCATATATATGTTATTTGGCGAGACATCAAATAAAGTTAACCATTTAAAAATTAAAA
AAAAAAAAAAA
Restriction Sites ECoRI-NOT     
ACCN NM_138448
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.
Reference Data
RefSeq NM_138448.2, NP_612457.1
RefSeq Size 1082 bp
RefSeq ORF 300 bp
Locus ID 98
UniProt ID P14621
Protein Pathways Pyruvate metabolism
Gene Summary Acylphosphatase can hydrolyze the phosphoenzyme intermediate of different membrane pumps, particularly the Ca2+/Mg2+-ATPase from sarcoplasmic reticulum of skeletal muscle. Two isoenzymes have been isolated, called muscle acylphosphatase and erythrocyte acylphosphatase on the basis of their tissue localization. This gene encodes the muscle-type isoform (MT). An increase of the MT isoform is associated with muscle differentiation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]
Transcript Variant: This variant (3) represents use of an alternate promoter and therefore differs in the 5' UTR and 5' coding region compared to variant 1. The resulting isoform (3) has a shorter and distinct N-terminus compared to 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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