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RNF170 antibody (AA 1-200)
RNF170
Reactivity: Mouse
WB
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-RNF170 Antibody
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Target
See all RNF170 Antibodies
RNF170
(Ring Finger Protein 170 (RNF170))
Binding Specificity
All epitopes for RNF170 antibodies
AA 1-200
Reactivity
All reactivities for RNF170 antibodies
Mouse
Host
All hosts for RNF170 antibodies
Rabbit
Clonality
All clonalities for RNF170 antibodies
Polyclonal
Conjugate
All conjugates for RNF170 antibodies
This RNF170 antibody is un-conjugated
Application
All applications for RNF170 antibodies
Western Blotting (WB)
Purpose
Rnf170 Rabbit pAb
Sequence
MQRYWRFQDN KIQDICFGVL GESWIQRPVM ARYYSEGQSL QQDDSFIEGV SDQVLVAVVV SLALTATLLY ALLRNVQQNI HPENQELVRV LREQFQTEQD VPAPARQQFY TEMYCPICLH QASFPVETNC GHLFCGSCII AYWRYGSWLG AISCPICRQT VTLLLTVFGE DDQSQDVIRL RQDVNDYNRR FSGQPRSIME
Cross-Reactivity
Mouse
Characteristics
Polyclonal Antibodies
Purification
Affinity purification
Immunogen
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 Primary Antibody
Alternatives
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Application Details
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Application Notes
WB,1:500 - 1:2000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for RNF170
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Target
RNF170
(Ring Finger Protein 170 (RNF170))
Alternative Name
Rnf170 (RNF170 Products )
Background
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
Molecular Weight
16kDa/24kDa/28kDa/33kDa
Gene ID
77733
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