Msx2/Hox8 antibody (N-Term)
Quick Overview for Msx2/Hox8 antibody (N-Term) (ABIN2777276)
Target
See all Msx2/Hox8 (Msx2) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- N-Term
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Sequence
- MASPSKGNDL FSPDEEGPAV VAGPGPGPGG AEGAAEERRV KVSSLPFSVE
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Predicted Reactivity
- Cow: 100%, Dog: 100%, Horse: 100%, Human: 100%, Mouse: 91%, Rabbit: 91%, Rat: 91%
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Characteristics
- This is a rabbit polyclonal antibody against MSX2. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the n terminal region of human MSX2
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
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Comment
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Antigen size: 267 AA
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- Lot specific
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Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handling Advice
- Avoid repeated freeze-thaw cycles.
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Storage
- -20 °C
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Storage Comment
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- Msx2/Hox8 (Msx2) (Msh Momeobox 2 (Msx2))
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Alternative Name
- MSX2
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Background
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MSX2 probable play a morphogenetic role. MSX2 may play a role in limb-pattern formation. In osteoblasts, MSX2 suppresses transcription driven by the osteocalcin FGF response element (OCFRE).This gene encodes a member of the muscle segment homeobox gene family. The encoded protein is a transcriptional repressor whose normal activity may establish a balance between survival and apoptosis of neural crest-derived cells required for proper craniofacial morphogenesis. The encoded protein may also have a role in promoting cell growth under certain conditions and may be an important target for the RAS signaling pathways. Mutations in this gene are associated with parietal foramina 1 and craniosynostosis type 2. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: CRS2, FPP, HOX8, MSH, PFM, PFM1
Protein Interaction Partner: ATXN1, PIAS2, UBC, XRCC5, XRCC6, ZDHHC2, TLE2, TLE1, PPARG, POU2AF1, NR3C1, POLR3D, SPEN, ZBTB17, RUNX2, DLX5, MAGED1, GTF2F2, GTF2F1, MSX1, DLX2, MSX2, CEBPA, PITX2,
Protein Size: 267 -
Molecular Weight
- 29 kDa
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Gene ID
- 4488
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NCBI Accession
- NM_002449, NP_002440
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UniProt
- P35548
Target
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