Anti-ALK-2 / ACVR1 antibody

Cat.#: 100080

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Product Information

  • Product Name
    Anti-ALK-2 / ACVR1 antibody
  • Documents
  • Description
    Rabbit polyclonal to ALK-2 / ACVR1
  • Tested applications
    ELISA, IHC-P
  • Species reactivity
    Human ALK-2 / ACVR1
  • Alternative names
    ACTRI antibody; FOP antibody; FOP antibody; ALK2 antibody; SKR1 antibody; TSRI antibody; ACTRI antibody; ACVR1A antibody; ACVRLK2 antibody; ALK2 antibody; Acvr antibody; Alk8 antibody; SKR1 antibody; Alk-2 antibody; Tsk7L antibody; ActR-I antibody; ActRIA antibody; Acvrlk2 antibody; D330013D15Rik antibody; ActR-I antibody; ActRIA antibody; Acvr antibody; ACVR1 antibody; Acvr1 antibody; ACVR1A antibody; Acvrlk2 antibody; ACVRLK2 antibody; ALK2 antibody; ALK2 antibody; Alk-2 antibody; Alk8 antibody; D330013D15Rik antibody; RP23-100B18.4 antibody; SKR1 antibody; SKR1 antibody; Tsk7L antibody; TSRI antibody
  • Immunogen
  • Isotype
    Rabbit IgG
  • Preparation
    Produced in rabbits immunized with purified, recombinant Human ALK-2 / ACVR1 (rh ALK-2 / ACVR1; Q04771; Met1-Val124). ALK-2 / ACVR1 specific IgG was purified by Human ALK-2 / ACVR1 affinity chromatography.
  • Clonality
    Polyclonal
  • Formulation
    0.2 μm filtered solution in PBS
  • Storage instructions
    This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free.
    Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles.
  • Applications

    ELISA:0.1-0.2 μg/mL

    This antibody can be used at 0.1-0.2 μg/mL with the appropriate secondary reagents to detect Human ALK-2 / ACVR1. The detection limit for Human ALK-2 / ACVR1 is < 0.039 ng/well.

    IHC-P: 0.1-2 μg/ml

  • Validations

    ALK-2 / ACVR1 Antibody, Rabbit PAb, Antigen Affinity Purified, Immunohistochemistry

    ALK-2 / ACVR1 Antibody, Rabbit PAb, Antigen Affinity Purified, Immunohistochemistry

    ALK-2 / ACVR1 Antibody, Rabbit PAb, Antigen Affinity Purified, Immunohistochemistry

    ALK-2 / ACVR1 Antibody, Rabbit PAb, Antigen Affinity Purified, Immunohistochemistry

  • Background
    ALK-2, also termed as ACVR1, was initially identified as an activin type I receptor because of its ability to bind activin in concert with ActRII or ActRIIB. ALK-2 is also identified as a BMP type I receptor. It has been demonstrated that ALK-2 forms complex with either the BMP-2/7-bound BMPR-II or ACVR2A /ACVR2B. ALK-1 and ALK-2 presenting in the yeast Saccharomyces cerevisiae are two haspin homologues. Both ALK-1 and ALK-2 exhibit a weak auto-kinase activity in vitro, and are phosphoproteins in vivo. ALK-1 and ALK-2 levels peak in mitosis and late-S/G2. Control of protein stability plays a major role in ALK-2 regulation. The half-life of ALK-2 is particularly short in G1. Overexpression of ALK-2, but not of ALK-1, causes a mitotic arrest, which is correlated to the kinase activity of the protein. This suggests a role for ALK-2 in the control of mitosis. Endoglin is phosphorylated on cytosolic domain threonine residues by the TGF-beta type I receptors ALK-2 and ALK-5 in prostate cancer cells. Endoglin did not inhibit cell migration in the presence of constitutively active ALK-2. Defects in ALK-2 are a cause of fibrodysplasia ossificans progressiva (FOP).
  • References
    • Armes NA,et al. (1997) The ALK-2 and ALK-4 activin receptors transduce distinct mesoderm-inducing signals during early Xenopus development but do not co-operate to establish thresholds. Development 124(19): 3797-804.
    • Armes NA, et al. (1999) A short loop on the ALK-2 and ALK-4 activin receptors regulates signaling specificity but cannot account for all their effects on early Xenopus development. J Biol Chem. 274(12):7929-35.
    • Kawai S, et al. (2000) Mouse smad8 phosphorylation downstream of BMP receptors ALK-2, ALK-3, and ALK-6 induces its association with Smad4 and transcriptional activity.Biochem Biophys Res Commun. 271(3):682-7.
    • Deng Y, et al. (2009) Efficient highly selective synthesis of methyl 2-(ethynyl)alk-2(E)-enoates and 2-(1'-chlorovinyl)alk-2(Z)-enoates from 2-(methoxycarbonyl)-2,3-allenols. Organic letters 11(10):2169-72.

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"