SIP1 antibody (mAb) (Clone 6E5)
Host / Isotype
Mouse / IgG2a
Reactivity
Human
Applications
ICC, IF, IHC, WB
CloneNo.
6E5
Cat No : 61095,61096 61095
Synonyms
Validation Data Gallery
Product Information
Tested Applications |
ICC, IF, IHC, WB
Applications Validated by Active Motif: WB: 1 - 4 ug/ml dilution |
Tested Reactivity | Human |
Host / Isotype | Mouse / IgG2a |
Class | Monoclonal |
Type | Antibody |
Immunogen | This SIP1 antibody was raised against a recombinant protein corresponding to amino acids 1-360 of human SIP1. |
Full Name | SIP1 antibody (mAb) (Clone 6E5) |
Synonyms | SIP1, Smad-interacting protein 1, ZEB2, Zinc finger E-box-binding homeobox 2, sequence-specific DNA binding protein, transcriptional repressor, embryonic development of neural structures, neural crest. delta-EF1/Zfh1 family of 2-handed zinc finger/homeodomain, SMAD1, SMAD2, SMAD3, CBX4, CTBP1, Hirschsprung disease, HSCR, clone 6E5, monoclonal, sample, dbdabs |
Molecular weight | 180 kDa |
GenBank accession number | NP_055610 |
RRID | AB_2614989 |
Purification Method | Protein G Chromatography |
Buffer | Purified IgG in 70 mM Tris (pH 8), 105 mM NaCl, 31 mM glycine, 0.07 mM EDTA, 30% glycerol and 0.035% sodium azide. Sodium azide is highly toxic. |
Storage | Some products may be shipped at room temperature. This will not affect their stability or performance. Avoid repeated freeze/thaw cycles by aliquoting items into single-use fractions for storage at -20°C for up to 2 years. Keep all reagents on ice when not in storage. |
Background Information
SIP1 (Smad-interacting protein 1, aka ZEB2, Zinc finger E-box-binding homeobox 2) is a sequence-specific DNA binding protein and transcriptional repressor that is involved in normal embryonic development of neural structures and the neural crest. SIP1 belongs to the delta-EF1/Zfh1 family of 2-handed zinc finger/homeodomain proteins and contains a SMAD-binding domain, a homeodomain and two clusters of zinc fingers on the N- and C-termini. SIP1 interacts directly with activated forms of SMAD1, SMAD2 and SMAD3, as well as CBX4 and CTBP1. Mutations in the SIP1 gene cause a form of Hirschsprung disease (HSCR).