WDR4 Antikörper
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- Target Alle WDR4 Antikörper anzeigen
- WDR4 (WD Repeat Domain 4 (WDR4))
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Reaktivität
- Human
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Wirt
- Maus
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Klonalität
- Monoklonal
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Konjugat
- Dieser WDR4 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)
- Produktmerkmale
- Homo sapiens WD repeat domain 4 (WDR4), transcript variant 2
- Aufreinigung
- Purified from mouse ascites fluids by affinity chromatography
- Immunogen
- Full length human recombinant protein of human WDR4(NP_387510) produced in HEK293T cell.
- Klon
- 4G1
- Isotyp
- IgG1
- Top Product
- Discover our top product WDR4 Primärantikörper
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- Applikationshinweise
- WB 1:2000, IF 1:100, FLOW 1:100,
- Kommentare
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The concentration of the product may vary between diferrent lots.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 0.5-1.0 mg/mL
- Buffer
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
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- Target
- WDR4 (WD Repeat Domain 4 (WDR4))
- Andere Bezeichnung
- WDR4 (WDR4 Produkte)
- Synonyme
- TRM82 antikoerper, TRMT82 antikoerper, AI415180 antikoerper, AI448349 antikoerper, D530049K22Rik antikoerper, WD repeat domain 4 antikoerper, WD repeat domain 4 S homeolog antikoerper, WDR4 antikoerper, Wdr4 antikoerper, wdr4.S antikoerper
- Hintergrund
- This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is excluded as a candidate for a form of nonsyndromic deafness (DFNB10), but is still a candidate for other disorders mapped to 21q22.3 as well as for the development of Down syndrome phenotypes. Two transcript variants encoding the same protein have been found for this gene.
- Molekulargewicht
- 45.3 kDa
- Gen-ID
- 10785
- NCBI Accession
- NM_033661
- HGNC
- 10785
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