WDR4 anticorps
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- Antigène Voir toutes WDR4 Anticorps
- WDR4 (WD Repeat Domain 4 (WDR4))
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Reactivité
- Humain
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Hôte
- Souris
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Clonalité
- Monoclonal
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Conjugué
- Cet anticorp WDR4 est non-conjugé
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Application
- Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)
- Attributs du produit
- Homo sapiens WD repeat domain 4 (WDR4), transcript variant 2
- Purification
- Purified from mouse ascites fluids by affinity chromatography
- Immunogène
- Full length human recombinant protein of human WDR4(NP_387510) produced in HEK293T cell.
- Clone
- 4G1
- Isotype
- IgG1
- Top Product
- Discover our top product WDR4 Anticorps primaire
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- Indications d'application
- WB 1:2000, IF 1:100, FLOW 1:100,
- Commentaires
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The concentration of the product may vary between diferrent lots.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.5-1.0 mg/mL
- Buffer
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
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- Antigène
- WDR4 (WD Repeat Domain 4 (WDR4))
- Autre désignation
- WDR4 (WDR4 Produits)
- Synonymes
- anticorps TRM82, anticorps TRMT82, anticorps AI415180, anticorps AI448349, anticorps D530049K22Rik, anticorps WD repeat domain 4, anticorps WD repeat domain 4 S homeolog, anticorps WDR4, anticorps Wdr4, anticorps wdr4.S
- Sujet
- 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.
- Poids moléculaire
- 45.3 kDa
- ID gène
- 10785
- NCBI Accession
- NM_033661
- HGNC
- 10785
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