FOXL2 (Human) Recombinant Protein (P01)
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More Files
- More Functions
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Specification
Product Description
Human FOXL2 full-length ORF ( NP_075555.1, 1 a.a. - 376 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
MMASYPEPEDAAGALLAPETGRTVKEPEGPPPSPGKGGGGGGGTAPEKPDPAQKPPYSYVALIAMAIRESAEKRLTLSGIYQYIIAKFPFYEKNKKGWQNSIRHNLSLNECFIKVPREGGGERKGNYWTLDPACEDMFEKGNYRRRRRMKRPFRPPPAHFQPGKGLFGAGGAAGGCGVAGAGADGYGYLAPPKYLQSGFLNNSWPLPQPPSPMPYASCQMAAAAAAAAAAAAAAGPGSPGAAAVVKGLAGPAASYGPYTRVQSMALPPGVVNSYNGLGGPPAAPPPPPHPHPHPHAHHLHAAAAPPPAPPHHGAAAPPPGQLSPASPATAAPPAPAPTSAPGLQFACARQPELAMMHCSYWDHDSKTGALHSRLDL
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
65.2
Interspecies Antigen Sequence
Mouse (94); Rat (93)
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Quality Control Testing
12.5% SDS-PAGE Stained with Coomassie Blue.
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 — FOXL2
Entrez GeneID
668GeneBank Accession#
NM_023067.2Protein Accession#
NP_075555.1Gene Name
FOXL2
Gene Alias
BPES, BPES1, PFRK, PINTO, POF3
Gene Description
forkhead box L2
Gene Ontology
HyperlinkGene Summary
This gene encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3. [provided by RefSeq
Other Designations
Blepharophimosis, epicanthus inversus, and ptosis 1|blepharophimosis, epicanthus inversus and ptosis|forkhead transcription factor FOXL2
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Interactome
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Disease
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