LHX4 Antikörper
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- Target Alle LHX4 Antikörper anzeigen
- LHX4 (LIM Homeobox 4 (LHX4))
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser LHX4 Antikörper ist unkonjugiert
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Applikation
- Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Kreuzreaktivität
- Human
- Aufreinigung
- Purified by antigen-affinity chromatography.
- Immunogen
- Recombinant protein encompassing a sequence within the center region of human Lhx4. The exact sequence is proprietary.
- Isotyp
- IgG
- Top Product
- Discover our top product LHX4 Primärantikörper
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- Applikationshinweise
- IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 0.65 mg/mL
- Buffer
- 0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal
- Konservierungsmittel
- Thimerosal (Merthiolate)
- Vorsichtsmaßnahmen
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- 4 °C,-20 °C
- Informationen zur Lagerung
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- Target
- LHX4 (LIM Homeobox 4 (LHX4))
- Andere Bezeichnung
- LIM homeobox 4 (LHX4 Produkte)
- Synonyme
- LHX4 antikoerper, si:dkeyp-35f11.3 antikoerper, CPHD4 antikoerper, A330062J17Rik antikoerper, Gsh-4 antikoerper, Gsh4 antikoerper, LIM homeobox 4 antikoerper, LIM homeobox protein 4 antikoerper, LHX4 antikoerper, lhx4 antikoerper, Lhx4 antikoerper
- Hintergrund
- LIM homeobox 4 , CPHD4,This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator and be involved in control of differentiation and development of the pituitary gland. Mutations in this gene are associated with syndromic short stature and pituitary and hindbrain defects. An alternative splice variant has been described but its biological nature has not been determined. [provided by RefSeq]
- Molekulargewicht
- 43 kDa
- Gen-ID
- 89884
- UniProt
- Q969G2
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