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Msx2/Hox8 antibody (AA 1-129)

This Rabbit Polyclonal antibody specifically detects Msx2/Hox8 in WB, ELISA and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN7598976

Quick Overview for Msx2/Hox8 antibody (AA 1-129) (ABIN7598976)

Target

See all Msx2/Hox8 (Msx2) Antibodies
Msx2/Hox8 (Msx2) (Msh Momeobox 2 (Msx2))

Reactivity

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  • 12
  • 5
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  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 49
  • 5
Rabbit

Clonality

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  • 4
Polyclonal

Conjugate

  • 28
  • 5
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  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Msx2/Hox8 antibody is un-conjugated

Application

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  • 32
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  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 8
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    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
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    AA 1-129

    Purpose

    Anti-Hox8/MSX2 Antibody Picoband®

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Characteristics

    Anti-Hox8/MSX2 Antibody Picoband® (ABIN7598976). Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human Hox8/MSX2 recombinant protein (Position: M1-M129).

    Isotype

    IgG
  • Application Notes

    Western blot, 0.25-0.5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Bernardini, L., Castori, M., Capalbo, A., Mokini, V., Mingarelli, R., Simi, P., Bertuccelli, A., Novelli, A., Dallapiccola, B. Syndromic craniosynostosis due to complex chromosome 5 rearrangement and MSX2 gene triplication. Am. J. Med. Genet. 143A: 2937-2943, 2007. 2. Davidson, D. The function and evolution of Msx genes: pointers and paradoxes. Trends Genet. 11: 405-411, 1995. 3. Florisson, J. M. G., Verkerk, A. J. M. H., Huigh, D., Hoogeboom, A. J. M., Swagemakers, S., Kremer, A., Heijsman, D., Lequin, M. H., Mathijssen, I. M. J., van der Spek, P. J. Boston type craniosynostosis: report of a second mutation in MSX2. Am. J. Med. Genet. 161A: 2626-2633, 2013.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Storage

    4 °C,-20 °C

    Storage Comment

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target

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

    Alternative Name

    MSX2

    Background

    Synonyms: Farnesyl pyrophosphate synthase, FPP synthase, FPS, (2E,6E)-farnesyl diphosphate synthase, Cholesterol-regulated 39 kDa protein, CR 39, Dimethylallyltranstransferase, Farnesyl diphosphate synthase, Geranyltranstransferase, Fdps

    Tissue Specificity: Expressed ubiquitously.

    Background: Homeobox protein MSX-2 is a protein that in humans is encoded by the MSX2 gene. 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.

    Molecular Weight

    37 kDa

    Gene ID

    4488

    UniProt

    P35548
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