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SEMA3E Antikörper (AA 401-450)

SEMA3E Reaktivität: Human, Maus WB, ELISA, ICC, IF (cc), IF (p), IHC (p), IHC (fro) Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN1387869
  • Target Alle SEMA3E Antikörper anzeigen
    SEMA3E (Sema Domain, Immunoglobulin Domain (Ig), Short Basic Domain, Secreted, (Semaphorin) 3E (SEMA3E))
    Bindungsspezifität
    • 14
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 401-450
    Reaktivität
    • 28
    • 21
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus
    Wirt
    • 26
    • 4
    • 3
    Kaninchen
    Klonalität
    • 30
    • 3
    Polyklonal
    Konjugat
    • 16
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser SEMA3E Antikörper ist unkonjugiert
    Applikation
    • 30
    • 12
    • 12
    • 11
    • 10
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    Kreuzreaktivität
    Human, Maus
    Homologie
    Rat,Cow,Sheep,Pig,Horse,Rabbit
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human SEMA3E/Semaphorin 3E
    Isotyp
    IgG
    Top Product
    Discover our top product SEMA3E Primärantikörper
  • Applikationshinweise
    WB 1:300-5000
    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    ICC 1:100-500
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    Konservierungsmittel
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    4 °C,-20 °C
    Informationen zur Lagerung
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Haltbarkeit
    12 months
  • Target
    SEMA3E (Sema Domain, Immunoglobulin Domain (Ig), Short Basic Domain, Secreted, (Semaphorin) 3E (SEMA3E))
    Andere Bezeichnung
    SEMA3E/Semaphorin 3E (SEMA3E Produkte)
    Synonyme
    M-SEMAH antikoerper, M-SemaK antikoerper, SEMAH antikoerper, coll-5 antikoerper, 6430702L12 antikoerper, AA408817 antikoerper, Semah antikoerper, mKIAA0331 antikoerper, semaphorin 3E antikoerper, sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E antikoerper, SEMA3E antikoerper, Sema3e antikoerper
    Hintergrund

    Synonyms: Coll 5, Coll5, KIAA0331, M sema H, M SEMAH, M SemaK, Msema H, MSEMAH, MSemaK, SEM3E_HUMAN, Sema domain immunoglobulin domain Ig, Sema domain immunoglobulin domain Ig short basic domain secreted 3E, Sema domain, immunoglobulin domain Ig, short basic domain, secreted, semaphorin 3E, SEMA3E, SEMAH, Semaphorin 3E, Semaphorin-3E, Semaphorin3E, Short basic domain secreted semaphorin 3E, SEM3E_HUMAN.

    Background: Semaphorins are a family of cell surface and secreted proteins involved in neural development that are conserved from insects to humans. Members of this family are approximately 750 amino acids in length (including signal sequences) and are defined by a conserved extracellular semaphorin? domain of approximately 500 amino acids containing 14-16 cysteines, blocks of conserved sequences and no obvious repeats. The transmembrane semaphorins are characterized by an additional 80 amino acid transmembrane domain and an 80-110 amino acid cytoplasmic domain. Secreted and cell-bound semaphorins chemically attract and repel the growth of neural axons, guiding the development of intricate networks of neural tissue. SEMA3E is a secreted semaphorin with 775 amino acids. Mutations in the SEMA3E gene are associated with CHARGE syndrome, a disorder characterized by cranial nerve dysfunction, coloboma of the eye, choanal atresia, inner and external ear abnormalities, cardiac anomalies, genitourinary abnormalities, and growth retardation.

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