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Histone H2A Variant (HIS2AV) (Internal Region), (pSer137) antibody

HIS2AV Reactivity: Drosophila melanogaster ELISA, WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN129671
  • Target See all Histone H2A Variant (HIS2AV) products
    Histone H2A Variant (HIS2AV)
    Binding Specificity
    Internal Region, pSer137
    Reactivity
    Drosophila melanogaster
    Host
    Rabbit
    Clonality
    Polyclonal
    Application
    ELISA, Western Blotting (WB)
    Specificity
    This affinity purified anti-Histone H2AvD pS137 Antibody is directed against the phosphorylated form of Drosophila H2AvD protein at the pS137 residue. The product was affinity purified from monospecific antiserum by immunoaffinity purification. Antiserum was first purified against the phosphorylated form of the immunizing peptide. The resultant affinity purified antibody was then cross-adsorbed against the non-phosphorylated form of the immunizing peptide. Reactivity occurs against Drosophila H2AvD pS137 protein and the antibody is specific for the phosphorylated form of the protein. Reactivity with non-phosphorylated Drosophila H2AvD is minimal by ELISA. A BLAST analysis was used to suggest little to no cross reactivity with H2AvD proteins from other sources based on a comparison using the immunizing sequence. Reactivity against homologues from other sources is not known.
    Characteristics
    Variant histones H2A are synthesized throughout the cell cycle and are very different from classical S-phase regulated H2A. H2AvD is vital for viability, but the exact function of variant histones H2A is not known. H2A is a core component of the nucleosome, an octamer containing two molecules each of H2A, H2B, H3 and H4. The octamer wraps approximately 146 bp of DNA. HsAvD is expressed both maternally and zygotically and is found in embryos through to adults (female only). The human homologue, H2AX, is phosphorylated by ATM protein kinase when double strand DNA breaks occur. In mouse, H2AX ''knock out'' mice have an increased incidence of cancer.
    Sterility
    Sterile filtered
    Immunogen
    Histone H2AvD pS137 Antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to amino acids 132-141 of Drosophila melanogaster (fruit fly) H2AvD protein.
    Immunogen Type: Peptide
    Isotype
    IgG
  • Application Notes
    Histone H2 AvD pS137 Antibody has been tested for use in ELISA and by western blot. Specific conditions for reactivity should be optimized by the end user. Expect a band approximately 14 kDa in size corresponding to phosphorylated H2 vD protein by western blotting in the appropriate Drosophila tissue or cell lysate or extract. Less than 0.2 % reactivity is observed against the non-phosphorylated form of the immunizing peptide. This antibody is phospho specific for pS137 of H2 vD protein.
    Comment

    Gene Name: HIS2AV

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.0 mg/ml
    Buffer
    0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
    Preservative
    Sodium azide
    Precaution of Use
    WARNING: Reagents contain sodium azide. Sodium azide is very toxic if ingested or inhaled. Avoid contact with skin, eyes, or clothing. Wear eye or face protection when handling. If skin or eye contact occurs, wash with copious amounts of water. If ingested or inhaled, contact a physician immediately. Sodium azide yields toxic hydrazoic acid under acidic conditions. Dilute azide-containing compounds in running water before discarding to avoid accumulation of potentially explosive deposits in lead or copper plumbing.
    Handling Advice
    Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store vial at 4 ° C prior to restoration. For extended storage aliquot contents and freeze at -24 ° C or below. This product is stable for several weeks at 4 ° C as an undiluted liquid. Dilute only prior to immediate use. Expiration date is one (1) year from date of opening.
    Expiry Date
    12 months
  • Lin, Wang, Lin, Rastegari, Su, Chang, Liao, Chang, Pi, Yu, Chen, Lin, Lu, Su, Tzou, Chan, Hsu: "Piwi reduction in the aged niche eliminates germline stem cells via Toll-GSK3 signaling." in: Nature communications, Vol. 11, Issue 1, pp. 3147, (2020) (PubMed).

    Perlmutter, Bordenstein, Unckless, LePage, Metcalf, Hill, Martinez, Jiggins, Bordenstein: "The phage gene wmk is a candidate for male killing by a bacterial endosymbiont." in: PLoS pathogens, Vol. 15, Issue 9, pp. e1007936, (2020) (PubMed).

    Grendler, Lowgren, Mills, Losick: "Wound-induced polyploidization is driven by Myc and supports tissue repair in the presence of DNA damage." in: Development (Cambridge, England), Vol. 146, Issue 15, (2020) (PubMed).

    Tsakiri, Gumeni, Vougas, Pendin, Papassideri, Daga, Gorgoulis, Juhász, Scorrano, Trougakos: "Proteasome dysfunction induces excessive proteome instability and loss of mitostasis that can be mitigated by enhancing mitochondrial fusion or autophagy." in: Autophagy, Vol. 15, Issue 10, pp. 1757-1773, (2020) (PubMed).

    Mlih, Khericha, Birdwell, West, Karpac: "A virus-acquired host cytokine controls systemic aging by antagonizing apoptosis." in: PLoS biology, Vol. 16, Issue 7, pp. e2005796, (2019) (PubMed).

    Cosolo, Jaiswal, Csordás, Grass, Uhlirova, Classen: "JNK-dependent cell cycle stalling in G2 promotes survival and senescence-like phenotypes in tissue stress." in: eLife, Vol. 8, (2019) (PubMed).

    Merigliano, Mascolo, La Torre, Saggio, Vernì: "Protective role of vitamin B6 (PLP) against DNA damage in Drosophila models of type 2 diabetes." in: Scientific reports, Vol. 8, Issue 1, pp. 11432, (2018) (PubMed).

    Harumoto, Lemaitre: "Male-killing toxin in a bacterial symbiont of Drosophila." in: Nature, Vol. 557, Issue 7704, pp. 252-255, (2018) (PubMed).

    McCarthy, Deiulio, Martin, Upadhyay, Rangan: "Tip60 complex promotes expression of a differentiation factor to regulate germline differentiation in female Drosophila." in: Molecular biology of the cell, Vol. 29, Issue 24, pp. 2933-2945, (2018) (PubMed).

    Caridi, DAgostino, Ryu, Zapotoczny, Delabaere, Li, Khodaverdian, Amaral, Lin, Rau, Chiolo: "Nuclear F-actin and myosins drive relocalization of heterochromatic breaks." in: Nature, Vol. 559, Issue 7712, pp. 54-60, (2018) (PubMed).

    Koehler, Perkins, Ellisman, Jones: "Pink1 and Parkin regulate Drosophila intestinal stem cell proliferation during stress and aging." in: The Journal of cell biology, Vol. 216, Issue 8, pp. 2315-2327, (2017) (PubMed).

    Merigliano, Marzio, Renda, Somma, Gatti, Vernì: "A Role for the Twins Protein Phosphatase (PP2A-B55) in the Maintenance of Drosophila Genome Integrity." in: Genetics, Vol. 205, Issue 3, pp. 1151-1167, (2017) (PubMed).

    Ma, Han, Song, Do, Yang, Ni, Xie: "DNA damage-induced Lok/CHK2 activation compromises germline stem cell self-renewal and lineage differentiation." in: Development (Cambridge, England), Vol. 143, Issue 23, pp. 4312-4323, (2017) (PubMed).

    Chen, Zheng, Xiao, Zheng: "Age-associated de-repression of retrotransposons in the Drosophila fat body, its potential cause and consequence." in: Aging cell, Vol. 15, Issue 3, pp. 542-52, (2017) (PubMed).

    Swenson, Colmenares, Strom, Costes, Karpen: "The composition and organization of Drosophila heterochromatin are heterogeneous and dynamic." in: eLife, Vol. 5, (2017) (PubMed).

    Delabaere, Ertl, Massey, Hofley, Sohail, Bienenstock, Sebastian, Chiolo, LaRocque: "Aging impairs double-strand break repair by homologous recombination in Drosophila germ cells." in: Aging cell, Vol. 16, Issue 2, pp. 320-328, (2017) (PubMed).

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    Upadhyay, Martino Cortez, Wong-Deyrup, Tavares, Schowalter, Flora, Hill, Nasrallah, Chittur, Rangan: "Transposon Dysregulation Modulates dWnt4 Signaling to Control Germline Stem Cell Differentiation in Drosophila." in: PLoS genetics, Vol. 12, Issue 3, pp. e1005918, (2016) (PubMed).

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  • Target
    Histone H2A Variant (HIS2AV)
    Alternative Name
    Histone H2AvD
    Synonyms
    5499 antibody, CG5499 antibody, Dmel\\CG5499 antibody, H2A antibody, H2A.F/Z antibody, H2A.X antibody, H2A.Z antibody, H2AV antibody, H2AV_DROM antibody, H2AX antibody, H2AZ antibody, H2Av antibody, H2AvD antibody, H2a.V antibody, H2av antibody, H2avD antibody, HIS antibody, HIS2AV antibody, HIS2AVD antibody, His antibody, His2 antibody, His2AV antibody, His2AvD antibody, HisH2Av antibody, Hist antibody, Hist2av antibody, gamma-H2Av antibody, gamma-HIS2AV antibody, gamma-His2Av antibody, gammaH2Av antibody, h2AvD antibody, his antibody, l(3)05146 antibody, l(3)810 antibody, l(3)97Dd antibody, l(3)L1602 antibody, Histone H2A variant antibody, His2Av antibody
    Background
    Variant histones H2A are synthesized throughout the cell cycle and are very different from classical S-phase regulated H2A. H2AvD is vital for viability, but the exact function of variant histones H2A is not known. H2A is a core component of the nucleosome, an octamer containing two molecules each of H2A, H2B, H3 and H4. The octamer wraps approximately 146 bp of DNA. HsAvD is expressed both maternally and zygotically and is found in embryos through to adults (female only). The human homologue, H2AX, is phosphorylated by ATM protein kinase when double strand DNA breaks occur. In mouse, H2AX ''knock out'' mice have an increased incidence of cancer.
    Synonyms: H2AvD protein antibody
    Gene ID
    43229, 17738227
    UniProt
    P08985
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