Polyclonal Rabbit anti-Human SLC5A11 / SMIT2 Antibody (WB)
Catalog Number: LS-C748223
2 sizes / from $281.00
Antibody: Rabbit Polyclonal
Applications: Immunohistochemistry (general), Western Blot
Reactivity: Human, Mouse, Rat
Format: Liquid
Western blot of Human HeLa. LAGE3 antibody dilution 1.0 ug/ml. This image was taken for the unconjugated form of this product. Other forms have not been tested.
Polyclonal Rabbit anti-Human LAGE3 Antibody (N-Terminus, WB)
Primary AntibodyLSBio Guarantee
| Antibody: | Rabbit Polyclonal |
| Applications: | Western Blot |
| Reactivity: | Human |
| Format: | Liquid |
$433.00each
Catalog Number: LS-C201798-100
Catalog Number: LS-C201798
For bulk orders or custom formulations:
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- Description
- LAGE3 antibody LS-C201798 is an unconjugated rabbit polyclonal antibody to human LAGE3 (N-Terminus). Validated for WB. Cited in 1 publication.
- Application
- WB
- Reactivity
- Hu
- Intended Use
- Research Use Only
- Guarantees
- This antibody carries the LSBio 100% Guarantee. ✓
- Category
- Antibodies > Primary Antibodies > Polyclonal Antibodies
- Alternative Names
- CVG5 | DXS9879E | DXS9951E | ESO3 | L antigen family, member 3 | L antigen family member 3 | Protein ESO-3 | ITBA2 | LAGE3 | Protein ITBA2
- UniProt Number
- Q14657
- NCBI GenBank
- NM_006014 | NP_006005.2
- SwissProt
- Q14657
Target
- Target
- Human LAGE3
- Antigen Species
- Human
- Epitope
- Human LAGE3
- Gene Name
- LAGE3
Antibody
- Host Species
- Rabbit
- Clonality
- Polyclonal
Immunogen
- Immunogen
- Synthetic peptide from N-Terminus of human LAGE3 (Q14657, NP_006005). Percent identity by BLAST analysis: Human (100%).
- Immunogen Type
- Synthetic Peptide (Linear)
Format
- Conjugate/Label
- Unconjugated
- Format
- Liquid
- Formulation
- PBS, 0.09% sodium azide, 2% sucrose
- Concentration
- 0.5 mg/mL
- Volume
- 100 Microliter
- Preservative
- Yes
- Purification Method
- Affinity Purified
Storage & Handling
- Storage Conditions
- Short term: Store at 2-8°C. Long term: Aliquot and store at -20°C. Avoid freeze/thaw cycles.
- Recommended Storage Buffer
- PBS
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, Boyer O, Revy P, Jobst-Schwan T, Schmidt JM, Lawson JA, Schanze D, Ashraf S, Ullmann JFP, Hoogstraten CA, Boddaert N, Collinet B, Martin G, Liger D, Lovric S, Furlano M, Guerrera IC, Sanchez-Ferras O, Hu JF, Boschat AC, Sanquer S, Menten B, Vergult S, De Rocker N, Airik M, Hermle T, Shril S, Widmeier E, Gee HY, Choi WI, Sadowski CE, Pabst WL, Warejko JK, Daga A, Basta T, Matejas V, Scharmann K, et al. Nature genetics. 2017 October;49:1529-1538. PubMed: 28805828 PMC: PMC5819591
