serum amyloid A2 (SAA2) (NM_030754) Human Untagged Clone

CAT#: SC122991

SAA2 (untagged)-Human serum amyloid A2 (SAA2), transcript variant 1


  "NM_030754" in other vectors (6)

Reconstitution Protocol

USD 310.00

In Stock*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol SAA2
Synonyms SAA; SAA1
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene sequence for NM_030754 edited
AGGGACCCGCAGCTCAGCTACAGCACAGATCAGCACCATGAAGCTTCTCACGGGCCTGGT
TTTCTGCTCCTTGGTCCTGAGTGTCAGCAGCCGAAGCTTCTTTTCGTTCCTTGGCGAGGC
TTTTGATGGGGCTCGGGACATGTGGAGAGCCTACTCTGACATGAGAGAAGCCAATTACAT
CGGCTCAGACAAATACTTCCATGCTCGGGGGAACTATGATGCTGCCAAAAGGGGACCTGG
GGGTGCCTGGGCCGCAGAAGTGATCAGCAATGCCAGAGAGAATATCCAGAGACTCACAGG
CCATGGTGCGGAGGACTCGCTGGCCGATCAGGCTGCCAATAAATGGGGCAGGAGTGGCAG
AGACCCCAATCACTTCCGACCTGCTGGCCTGCCTGAGAAATACTGAGCTTCCTCTTCACT
CTGCTCTCAGGAGACCTGGCTATGAGGCCCTCGGGGCAGGGATACAAAGTTAGTGAGGTC
TATGTCCAGAGAAGCTGAGATATGGCATATAATAGGCATCTAATAAATGCTTAAGAGGTC
AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
>OriGene 5' read for NM_030754 unedited
NNNGGTACCGTACAAAATTGTATACGACTCACTATAGGCGGCCGCGNAATTCGCCATTAC
GGCCGGGGAGGGACCCGCAGCTCAGCTACAGCACAGATCAGCACCATGAAGCTTCTCACG
GGCCTGGTTTTCTGCTCCTTGGTCCTGAGTGTCAGCAGCCGAAGCTTCTTTTCGTTCCTT
GGCGAGGCTTTTGATGGGGCTCGGGACATGTGGAGAGCCTACTCTGACATGAGAGAAGCC
AATTACATCGGCTCAGACAAATACTTCCATGCTCGGGGGAACTATGATGCTGCCAAAAGG
GGACCTGGGGGTGCCTGGGCCGCAGAAGTGATCAGCAATGCCAGAGAGAATATCCAGAGA
CTCACAGGCCATGGTGCGGAGGACTCGCTGGCCGATCAGGCTGCCAATAAATGGGGCAGG
AGTGGCAGAGACCCCAATCACTTCCGACCTGCTGGCCTGCCTGAGAAATACTGAGCTTCC
TCTTCACTCTGCTCTCAGGAGACCTGGCTATGAGGCCCTCGGGGCAAGGATACAAAGTTA
GTGAGGTCTATGTCCAGAGAAGCTGAGATATGGCATATAATAAGGCATCTAATAAATGCT
TAAGAAGGTCAAAAANANNNNAAAAANAAAAAAAAAACATGTCGGCCGGCTCGGGCCTTG
ACTTTAGATTGCGGCCCCGGCCTAAACTGTTTCCTGAACAATCCCCGGGTGCATCCCTGG
TAACCCTCCCCATGGCCTTCCTGGGCCTGGGAATTTCCCCTTCCTTGCCCCCCACCCTTG
CCCAAAAAAAATAAATTGCCCCATTTGCCCACAAAGGGGT
Restriction Sites Please inquire     
ACCN NM_030754
Insert Size 570 bp
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.
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_030754.2, NP_110381.1
RefSeq Size 526 bp
RefSeq ORF 369 bp
Locus ID 6289
Cytogenetics 11p15.1
Protein Families Druggable Genome
Gene Summary 'This gene encodes a member of the serum amyloid A family of apolipoproteins. The encoded preproprotein is proteolytically processed to generate the mature protein. This protein is a major acute phase protein that is highly expressed in response to inflammation and tissue injury. This protein also plays an important role in HDL metabolism and cholesterol homeostasis. High levels of this protein are associated with chronic inflammatory diseases including atherosclerosis, rheumatoid arthritis, Alzheimer's disease and Crohn's disease. This protein may also be a potential biomarker for certain tumors. Finally, antimicrobial activity against S. aureus and E. coli resides in the N-terminal portion of the mature protein. [provided by RefSeq, Jul 2020]'
Transcript Variant: This variant (1) encodes the longer isoform (a). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.

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