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Product Name
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Smad Interacting Protein 1 antibody
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See all Smad Interacting Protein 1 antibodies (2)...
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Product type
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Primary antibodies
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Description
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Rabbit polyclonal to Smad Interacting Protein 1
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Note on antibody grade |
Fast-Track antibodies
- Immunogen affinity purified
- high ELISA titre values
- released early (to accelerate your research)
- 950 Abpoints to the 1st researcher
who submits conclusive data (positive or negative): Read the Fast-Track antibody Terms of Use
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Immunogen
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Synthetic peptide conjugated to KLH derived from within residues 1100 - 1200 of Human Smad Interacting Protein 1.
(Peptide available as ab32699.)
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Predicted to react
(species key)
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Hu, Ms, Rat (Due to sequence homology)
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Abreviews
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Application notes
(see key)
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Recommended dilutions This antibody gave a positive result in ELISA against the immunizing peptide (ab32699). Not yet tested in other applications.
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Cellular localization
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Nuclear
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Research areas
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Developmental Biology >> Lineage specification >> Ectoderm Cancer >> Oncoproteins/suppressors >> Oncoproteins >> Transcription factors Chromatin and Nuclear Signaling >> Nuclear Signaling Pathways >> SMADs Stem Cells >> Lineage Markers >> Ectoderm Chromatin and Nuclear Signaling >> Transcription >> Domain Families >> Developmental Families >> Other Neuroscience >> Neurology process >> Neurogenesis Chromatin and Nuclear Signaling >> Transcription >> Domain Families >> Zinc Finger
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Relevance
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Smad Interacting Protein 1 (SIP1) is observed in neural crest derived cells (peripheric nervous system, enteric nervous system, facial neurectoderm and cranial nerve ganglia), central nervous system, genital tubercle, muscles and kidneys in the developing human. 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 can be induced by TGF. SIP1 plays a crucial role in normal embryonic development of neural structures and the neural crest. Mutations in the SIP1 gene cause a form of Hirschsprung disease (HSCR). Patients with SIP1 mutations show mental retardation, delayed motor development, epilepsy, microcephaly, distinct facial features and/or congenital heart disease. SIP1 is also involved in the regulation of epithelial to mesenchymal transition, an important process in tumor progression.
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Database links
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The links below go to external sites and will open in a new browser window
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Raised in
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Rabbit
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Clonality
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Polyclonal
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Isotype
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IgG
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Purity
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Immunogen affinity purified
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Storage buffer
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Preservative: 0.02% Sodium Azide Constituents: 1% BSA, PBS. pH 7.4 Material safety datasheet (MSDS) for this product: Sodium Azide MSDS
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Form
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Liquid
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Concentration
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Batch dependent within range: 0.10 - 1.00 mg/ml
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Storage instructions
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Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
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At Abcam, we have one centralized database to hold all of our product information, so that everything we know about this Smad Interacting Protein 1 antibody is on this datasheet. But please do contact us if you would like any reassurance! |
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Search PubMed (MEDLINE) for references to Smad Interacting Protein 1
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Smad Interacting Protein 1 antibody - more information
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Customer reviews (feedback) regarding Smad Interacting Protein 1 antibody |
Customer FAQs regarding Smad Interacting Protein 1 antibody |
Protocols for Smad Interacting Protein 1 antibody |
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Contact Abcam with a Technical Enquiry about Smad Interacting Protein 1 antibody |
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All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"