Msx2/Hox8 antibody (AA 1-267)

Catalog No. ABIN3015839

Product Details anti-Msx2/Hox8 Antibody

Target: Msx2/Hox8 (Msx2) (Msh Momeobox 2 (Msx2))

Binding Specificity: AA 1-267

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Msx2/Hox8 antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: MASPSKGNDL FSPDEEGPAV VAGPGPGPGG AEGAAEERRV KVSSLPFSVE ALMSDKKPPK EASPLPAESA SAGATLRPLL LSGHGAREAH SPGPLVKPFE TASVKSENSE DGAAWMQEPG RYSPPPRHMS PTTCTLRKHK TNRKPRTPFT TSQLLALERK FRQKQYLSIA ERAEFSSSLN LTETQVKIWF QNRRAKAKRL QEAELEKLKM AAKPMLPSSF SLPFPISSPL QAASIYGASY PFHRPVLPIP PVGLYATPVG YGMYHLS

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-267 of human MSX2 (NP_002440.2).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Restrictions: For Research Use only

Handling

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for Msx2/Hox8

Target: Msx2/Hox8 (Msx2) (Msh Momeobox 2 (Msx2))

Alternative Name: MSX2 (Msx2 Products)

Synonyms: CRS2 antibody, FPP antibody, HOX8 antibody, MSH antibody, PFM antibody, PFM1 antibody, BB122635 antibody, Hox-8 antibody, Hox8 antibody, Hox8.1 antibody, HOX-8 antibody, Msx-2 antibody, msh homeobox 2 antibody, MSX2 antibody, Msx2 antibody

Background: 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.,MSX2,CRS2,FPP,HOX8,MSH,PFM,PFM1,Epigenetics & Nuclear Signaling,Transcription Factors,Cancer,Signal Transduction,Neuroscience,Cardiovascular,Heart,Cardiogenesis,MSX2

Molecular Weight: 28 kDa

Gene ID: 4488

UniProt: P35548