Anti RBM4 pAb (ATL-HPA047849)
Atlas Antibodies
- Catalog No.:
- ATL-HPA047849-25
![Lane 1: Marker [kDa] 250, 130, 95, 72, 55, 36, 28, 17, 10<br/>Lane 2: Human cell line RT-4<br/>Lane 3: Human cell line U-251MG sp<br/>Lane 4: Human plasma (IgG/HSA depleted)<br/>Lane 5: Human liver tissue<br/>Lane 6: Human tonsil tissue](https://cdn11.bigcommerce.com/s-ydswqc5qsc/images/stencil/640x640/products/94130/171240/atl-hpa047849_anti-rbm4-pab-atl-hpa047849_52892__26424.1681125076.jpg?c=2 "Lane 1: Marker [kDa] 250, 130, 95, 72, 55, 36, 28, 17, 10<br/>Lane 2: Human cell line RT-4<br/>Lane 3: Human cell line U-251MG sp<br/>Lane 4: Human plasma (IgG/HSA depleted)<br/>Lane 5: Human liver tissue<br/>Lane 6: Human tonsil tissue")
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- Calculated at Checkout
$303.00
Gene Name: RBM4
Alternative Gene Name: LARK, RBM4A, ZCCHC21, ZCRB3A
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000033760: 93%, ENSRNOG00000061795: 98%
Entrez Gene ID: 5936
Uniprot ID: Q9BWF3
Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage Temperature: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
| Product Specifications | |
| Application | WB, ICC, IHC |
| Reactivity | Human |
| Clonality | Polyclonal |
| Host | Rabbit |
| Immunogen | PTVGEGYGYGPESELSQASAATRNSLYDMARYEREQYVDRARYSA |
| Gene Sequence | PTVGEGYGYGPESELSQASAATRNSLYDMARYEREQYVDRARYSA |
| Gene ID - Mouse | ENSMUSG00000033760 |
| Gene ID - Rat | ENSRNOG00000061795 |
| Buffer | 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative. |
| Documents & Links for Anti RBM4 pAb (ATL-HPA047849) | |
| Datasheet | Anti RBM4 pAb (ATL-HPA047849) Datasheet (External Link) |
| Vendor Page | Anti RBM4 pAb (ATL-HPA047849) at Atlas Antibodies |
| Documents & Links for Anti RBM4 pAb (ATL-HPA047849) | |
| Datasheet | Anti RBM4 pAb (ATL-HPA047849) Datasheet (External Link) |
| Vendor Page | Anti RBM4 pAb (ATL-HPA047849) |
| Citations for Anti RBM4 pAb (ATL-HPA047849) – 1 Found |
| Vihola, Anna; Palmio, Johanna; Danielsson, Olof; Penttilä, Sini; Louiselle, Daniel; Pittman, Sara; Weihl, Conrad; Udd, Bjarne. Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression. Neurology. Genetics. 2019;5(3):e337. PubMed |