Validation Data Gallery
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Tested Applications
| Positive WB detected in | HEK-293 cells, L02 cells, NIH/3T3 cells |
Recommended dilution
| Application | Dilution |
|---|---|
| Western Blot (WB) | WB : 1:5000-1:50000 |
| It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
| Sample-dependent, Check data in validation data gallery. | |
Product Information
84320-2-RR targets VIPAS39 in WB, ELISA applications and shows reactivity with human, mouse samples.
| Tested Reactivity | human, mouse |
| Host / Isotype | Rabbit / IgG |
| Class | Recombinant |
| Type | Antibody |
| Immunogen | VIPAS39 fusion protein Ag14762 相同性解析による交差性が予測される生物種 |
| Full Name | chromosome 14 open reading frame 133 |
| Calculated molecular weight | 493 aa, 57 kDa |
| Observed molecular weight | 50 kDa |
| GenBank accession number | BC015054 |
| Gene Symbol | VIPAS39 |
| Gene ID (NCBI) | 63894 |
| RRID | AB_3671861 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Purification Method | Protein A purification |
| UNIPROT ID | Q9H9C1 |
| Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol , pH 7.3 |
| Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
Background Information
VIPAS39 (also known as C14orf133 or SPE-39) is a binding protein to Vps33B, one of the subunits in the mammalian HOPS complex. VIPAS39 may be involved in endosomal maturation or fusion (PMID: 23918659). Mutations in Vps33B and VIPAS39 cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome, which is a rare autosomal recessive multisystem disorder associated with abnormalities in polarized liver and kidney cells (PMID: 20190753).
Protocols
| Product Specific Protocols | |
|---|---|
| WB protocol for VIPAS39 antibody 84320-2-RR | Download protocol |
| Standard Protocols | |
|---|---|
| Click here to view our Standard Protocols |