product summary
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company name :
MyBioSource
product type :
cDNA
product name :
SETBP1 cDNA Clone
catalog :
MBS1273301
quantity :
0.01 mg Plasmid + 0.
price :
165 USD
more info or order :
product information
catalog number :
MBS1273301
products type :
cDNA Clone
products full name :
SETBP1 cDNA Clone
products short name :
SETBP1
other names :
Homo sapiens SET binding protein 1, mRNA; SET-binding protein; SET-binding protein; SET binding protein 1
products gene name :
SETBP1
other gene names :
SETBP1; SETBP1; SEB; MRD29; KIAA0437; SEB
uniprot entry name :
SETBP_HUMAN
sequence length :
1804
sequence :
atggagtccagggaaaccttaagcagctcccggcaaaga
gggggcgagtcagacttcctgccggtctcctcagccaag
cccccagctgctcctggctgtgcaggagaacctttgctc
tccactccaggacctgggaaggggatcccggtgggcgga
gagcgcatggagccagaggaggaggatgaactaggctca
gggcgggatgtggattccaactccaacgcggacagtgag
aaatgggtggcaggagatggtttggaagagcaggaattt
tctatcaaggaggcaaacttcacagagggaagtctgaag
ctaaagattcagaccacaaagcgggctaagaaaccccca
aagaatttggagaactatatatgtccacctgagatcaag
atcaccatcaagcagtctggggaccagaaggtgtcccgt
gctggaaaaaatagcaaagccacgaaggaggaagaaaga
agccactccaaaaagaagctcctcacagccagtgacctt
gcagccagtgacctcaaaggatttcagccacagattaaa
gactccagtaaggaggaagtctggaagagaagaggaggc
caaggcatcccattcaaaaagcaattcctgtcccaggaa
cgtgccatgtgcttctcatgcccccggaacccattcccc
gcaaaacccggttctctcactcttccttttcacagtgaa
cctgcagtctgggcacaagaagtataa
other info1 :
Vector: Please Inquire
ncbi gi num :
38382763
ncbi acc num :
BC062338
ncbi mol weight :
26,397 Da
ncbi summary :
This gene encodes a protein which contains a several motifs including a ski homology region and a SET-binding region in addition to three nuclear localization signals. The encoded protein has been shown to bind the SET nuclear oncogene which is involved in DNA replication. Mutations in this gene are associated with Schinzel-Giedion midface retraction syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]
uniprot summary :
SETBP1: Defects in SETBP1 are the cause of Schinzel-Giedion midface retraction syndrome (SGMFS). It is a disorder characterized by severe mental retardation, distinctive facial features, and multiple congenital malformations including skeletal abnormalities, genitourinary and renal malformations, cardiac defects, as well as a higher-than-normal prevalence of tumors, notably neuroepithelial neoplasia. 2 isoforms of the human protein are produced by alternative splicing. Protein type: Unknown function. Chromosomal Location of Human Ortholog: 18q21.1. Molecular Function: protein binding. Disease: Mental Retardation, Autosomal Dominant 29; Schinzel-giedion Midface Retraction Syndrome
size1 :
0.01 mg Plasmid + 0.2 mL Glycerol-Stock
price1 :
165 USD
more info or order :
company information
MyBioSource
P.O. Box 153308
San Diego, CA 92195-3308
sales@mybiosource.com
https://www.mybiosource.com
1-888-627-0165
headquarters: USA
MyBioSource, LLC was orginally founded in Vancouver by three enthusiastic scientists who are passionate about providing the world with the best reagents available. Together, they form a company with a big vision known as MyBioSource. MyBioSource is now located in San Diego, California, USA.

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