Anti-RNF135 Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,WB,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-RNF135 Antibody (CSB-PA811599ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

E3 ubiquitin-protein ligase RNF135 Antibody,RIG-I E3 ubiquitin ligase Antibody,REUL Antibody,RING finger protein 135 Antibody,Riplet Antibody,RNF135 Antibody,L13 Antibody

More alternative names for the antibody
E3 ubiquitin-protein ligase RNF135 antibody|L13 antibody|MGC13061 antibody|MMFD antibody|REUL antibody|RIG-I E3 ubiquitin ligase antibody|RING finger protein 135 antibody|Riplet antibody|RN135_HUMAN antibody|Rnf135 antibody
Anti-RNF135 antibody (ab28636)
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Recommended applications: ELISA, WB, IHC

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-RNF135 Antibody

Catalogue No.

CSB-PA811599ESR2HU

Reactivity

Human

Immunogen

Recombinant human E3 ubiquitin-protein ligase RNF135 protein (339-432AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

47 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:84282( Human), Entrez Gene:71956( Mouse), Omim:611358( Human), SwissProt:Q8IUD6( Human), SwissProt:Q9CWS1( Mouse), Unigene:29874( Human), Unigene:22985( Mouse)

Protein function

Acts as an E2-dependent E3 ubiquitin-protein ligase, involved in innate immune defense against viruses. Ubiquitinates DDX58 and is required for full activation of the DDX58 signaling resulting in interferon beta production. .

Protein tissue specificity

Expressed in skeletal muscle, spleen, kidney, placenta, prostate, stomach, thyroid and tongue. Also weakly expressed in heart, thymus, liver and lung. .

Involvement in disease

Macrocephaly, macrosomia, facial dysmorphism syndrome (MMFD) [MIM:614192]: An autosomal dominant disorder characterized by the association of macrothrombocytopathy and progressive sensorineural hearing loss without renal dysfunction. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein cellular localization

Cytoplasm .

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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