MKS1 (Human) Recombinant Protein (P01)
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More Files
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Specification
Product Description
Human MKS1 full-length ORF ( AAH10061.1, 1 a.a. - 377 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
MTTAASEVPSFLVERMANVRRRRQDRRGMEGGILKSRIVTWEPSEEFVRNNHVINTPLQTMHIMADLGPYKKLGYKKYEHVLCTLKVDSNGVITVKPDFTGLKGPYRIETEGEKQELWKYTIDNVSPHAQPEEEERERRVFKDLYGRHKEYLSSLVGTDFEMTVPGALRLFVNGEVVSAQGYEYDNLYVHFFVELPTAHWSSPAFQQLSGVTQTCTTKSLAMDKVAHFSYPFTFEAFFLHEDESSDALPEWPVLYCEVLSLDFWQRYRVEGYGAVVLPATPGSHTLTVSTWRPVELGTVAELRRFFIGGSLELEDLSYVRIPGSFKGLSSSKTKEGRKVDGERVLNPQPVSLSLFPGKPHSTAWGLLRLRYELFLSK
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
69.4
Interspecies Antigen Sequence
Mouse (87); Rat (85)
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Storage Buffer
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Enzyme-linked Immunoabsorbent Assay
Western Blot (Recombinant protein)
Antibody Production
Protein Array
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Gene Info — MKS1
Entrez GeneID
54903GeneBank Accession#
BC010061.2Protein Accession#
AAH10061.1Gene Name
MKS1
Gene Alias
BBS13, FLJ20345, MES, MKS
Gene Description
Meckel syndrome, type 1
Gene Ontology
HyperlinkGene Summary
The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
Other Designations
FABB proteome-like protein
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Interactome
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Disease
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