EVX2 polyclonal antibody
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More Files
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of human colon with EVX2 polyclonal antibody (Cat # PAB23830) shows strong cytoplasmic positivity in glandular cells.
Immunofluorescence
Immunofluorescent staining of human cell line A-431 with EVX2 polyclonal antibody (Cat # PAB23830) at 1-4 ug/mL dilution shows positivity in nucleus but not nucleoli.
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Specification
Product Description
Rabbit polyclonal antibody raised against recombinant EVX2.
Immunogen
Recombinant protein corresponding to amino acids of human EVX2.
Sequence
PLHSALGELPAKGKFEIDTLFNLQHTGSESTVSSEISSAAESRKKPGHYS
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Antigen affinity purification
Isotype
IgG
Recommend Usage
Immunohistochemistry (1:50-1:200)
Immunofluorescence (1-4 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.2 (40% glycerol, 0.02% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of human colon with EVX2 polyclonal antibody (Cat # PAB23830) shows strong cytoplasmic positivity in glandular cells.Immunofluorescence
Immunofluorescent staining of human cell line A-431 with EVX2 polyclonal antibody (Cat # PAB23830) at 1-4 ug/mL dilution shows positivity in nucleus but not nucleoli. -
Gene Info — EVX2
Entrez GeneID
344191Protein Accession#
Q03828Gene Name
EVX2
Gene Alias
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Gene Description
even-skipped homeobox 2
Omim ID
142991Gene Ontology
HyperlinkGene Summary
This gene is located at the 5' end of the HOXD gene cluster on chromosome 2. The encoded protein is a homeobox transcription factor that is related to the protein encoded by the Drosophila even-skipped (eve) gene, a member of the pair-rule class of segmentation genes. A 117 kb microdeletion at the 5' end of the HOXD gene cluster, which includes this gene and the HOXD9-HOXD13 genes, causes synpolydactyly, a dominantly inherited disease resulting in limb malformation. [provided by RefSeq
Other Designations
Even-skipped homeo box-2|eve, even-skipped homeo box homolog 2|eve, even-skipped homeobox homolog 2|even-skipped homeo box 2 (homolog of Drosophila eve)
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