RNF170 anticorps (AA 1-200)
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- Antigène Voir toutes RNF170 Anticorps
- RNF170 (Ring Finger Protein 170 (RNF170))
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Épitope
- AA 1-200
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Reactivité
- Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp RNF170 est non-conjugé
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Application
- Western Blotting (WB)
- Fonction
- Rnf170 Rabbit pAb
- Séquence
- MQRYWRFQDN KIQDICFGVL GESWIQRPVM ARYYSEGQSL QQDDSFIEGV SDQVLVAVVV SLALTATLLY ALLRNVQQNI HPENQELVRV LREQFQTEQD VPAPARQQFY TEMYCPICLH QASFPVETNC GHLFCGSCII AYWRYGSWLG AISCPICRQT VTLLLTVFGE DDQSQDVIRL RQDVNDYNRR FSGQPRSIME
- Réactivité croisée
- Souris
- Attributs du produit
- Polyclonal Antibodies
- Purification
- Affinity purification
- Immunogène
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-200 of mouse Rnf170 (NP_084241.1).
- Isotype
- IgG
- Top Product
- Discover our top product RNF170 Anticorps primaire
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- Indications d'application
- WB,1:500 - 1:2000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 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
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- RNF170 (Ring Finger Protein 170 (RNF170))
- Autre désignation
- Rnf170 (RNF170 Produits)
- Synonymes
- anticorps SNAX1, anticorps 6720407G21Rik, anticorps AI481227, anticorps ring finger protein 170, anticorps ring finger protein 170 L homeolog, anticorps microRNA 4469, anticorps Rnf170, anticorps RNF170, anticorps rnf170.L, anticorps MIR4469
- Sujet
- This gene encodes a RING domain-containing protein that resides in the endoplasmic reticulum (ER) membrane. This protein functions as an E3 ubiquitin ligase and mediates ubiquitination and processing of inositol 1,4,5-trisphosphate (IP3) receptors via the ER-associated protein degradation pathway. It is recruited to the activated IP3 receptors by the ERLIN1/ERLIN2 complex to which it is constitutively bound. Mutations in this gene are associated with autosomal dominant sensory ataxia. Alternatively spliced transcript variants have been found for this gene.,RNF170,ADSA,SNAX1,Rnf170,Cell Biology & Developmental Biology,Rnf170
- Poids moléculaire
- 16kDa/24kDa/28kDa/33kDa
- ID gène
- 77733
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