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HECW1 rabbit pAb

Function: E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent degradation of DVL1. Also targets the mutant SOD1 protein involved in familial amyotrophic lateral sclerosis (FALS). Forms cytotoxic aggregates with DVL1, SSR3 and mutant SOD1 that lead to motor neuron death in FALS. pathway: Protein modification; protein ubiquitination. similarity: Contains 1 C2 domain. similarity: Contains 1 HECT (E6AP-type E3 ubiquitin-protein ligase) domain. similarity: Contains 2 WW domains. subunit: Interacts with DVL1 and SSR3. Also interacts with mutant SOD1. tissue specificity: Predominantly expressed in neurons of adult and fetal brain. Weakly expressed in the kidney.

Product Specifications

Background

Function:E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent degradation of DVL1. Also targets the mutant SOD1 protein involved in familial amyotrophic lateral sclerosis (FALS) . Forms cytotoxic aggregates with DVL1, SSR3 and mutant SOD1 that lead to motor neuron death in FALS., pathway:Protein modification; protein ubiquitination., similarity:Contains 1 C2 domain., similarity:Contains 1 HECT (E6AP-type E3 ubiquitin-protein ligase) domain., similarity:Contains 2 WW domains., subunit:Interacts with DVL1 and SSR3. Also interacts with mutant SOD1., tissue specificity:Predominantly expressed in neurons of adult and fetal brain. Weakly expressed in the kidney.

UniProt

Q76N89

Swiss Prot

Q76N89

Reactivity

Human; Rat; Mouse

Immunogen

Synthesized peptide derived from part region of human protein. AA range: 1-67

Clonality

Polyclonal

Source

Rabbit

Applications

WB; ELISA

Concentration

1 mg/ml

Dilution

WB 1:500-2000 ELISA 1:5000-20000

Molecular Weight

176kD

Storage Conditions

-20°C/1 year

Observed Molecular Weight

176kD

Fragment

IgG

Subcellular Location

Cytoplasm .

Gene ID (Human)

23072

Available Sizes

Curated Selection

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