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MOSPD2 antibody (AA 111-496)

MOSPD2 Reactivity: Human, Mouse, Rat WB, IHC, ELISA, FACS Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7599743
  • Target See all MOSPD2 products
    MOSPD2 (Motile Sperm Domain Containing 2 (MOSPD2))
    Binding Specificity
    • 8
    • 4
    • 3
    • 1
    • 1
    AA 111-496
    Reactivity
    • 13
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 12
    • 1
    Rabbit
    Clonality
    • 12
    • 1
    Polyclonal
    Conjugate
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    This MOSPD2 antibody is un-conjugated
    Application
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)
    Purpose
    Anti-MOSPD2 Antibody Picoband®
    Cross-Reactivity (Details)
    No cross-reactivity with other proteins.
    Characteristics
    Anti-MOSPD2 Antibody Picoband® (ABIN7599743). Tested in ELISA, IHC, WB, Flow Cytometry applications. This antibody reacts with Human, Mouse, Rat. 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 MOSPD2 recombinant protein (Position: R111-Q496).
    Isotype
    IgG
  • Application Notes
    Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
    Immunohistochemistry, 2-5 μg/mL, Human, Mouse, Rat
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Di Mattia, T., Martinet, A., Ikhlef, S., McEwen, A. G., Nomine, Y., Wendling, C., Poussin-Courmontagne, P., Voilquin, L., Eberling, P., Ruffenach, F., Cavarelli, J., Slee, J., Levine, T. P., Drin, G., Tomasetto, C., Alpy, F. FFAT motif phosphorylation controls formation and lipid transfer function of inter-organelle contacts. EMBO J. 39: e104369, 2020. 2. Di Mattia, T., Wilhelm, L. P., Ikhlef, S., Wendling, C., Spehner, D., Nomine, Y., Giordano, F., Mathelin, C., Drin, G., Tomasetto, C., Alpy, F. Identification of MOSPD2, a novel scaffold for endoplasmic reticulum membrane contact sites. EMBO Rep. 19: e45453, 2018. 3. Mendel, I., Yacov, N., Salem, Y., Propheta-Meiran, O., Ishai, E., Breitbart, E. Identification of motile sperm domain-containing protein 2 as regulator of human monocyte migration. J. Immun. 198: 2125-2132, 2017.
    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
    MOSPD2 (Motile Sperm Domain Containing 2 (MOSPD2))
    Alternative Name
    MOSPD2 (MOSPD2 Products)
    Background

    Synonyms: Kelch repeat and BTB domain-containing protein 2, BTB and kelch domain-containing protein 1, KBTBD2, BKLHD1, KIAA1489

    Tissue Specificity: Detected in liver, skeletal muscle, kidney, pancreas, spleen, thyroid, testis, ovary, small intestine and colon.

    Background: MOSPD2 (motile sperm domain-containing protein 2) is a 518 amino acid single-pass membrane protein that contains one CRAL-TRIO domain and a single MSP domain. Existing as two alternatively spliced isoforms, MOSPD2 is encoded by a gene that maps to human chromosome Xp22.2. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

    Molecular Weight
    60 kDa
    Gene ID
    158747
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