Price range: $268.00 through $328.00
Background:
This gene encodes a zinc finger transcription factor thought to play a role in the development of abducens motor neurons. Defects in this gene are a cause of Duane-radial ray syndrome (DRRS). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015],
| Size | 50μL/100μL |
| Target | SALL4 |
| Reactivity | Human |
| Applications | IHC, WB, IF, ELISA |
| MW(Calculated) | 113kD |
| MW(Observed) | 130kD |
| Host Species | Mouse |
| Isotype | IgG2b,Kappa |
| Conjugate/Modification | Unmodified |
| Recommended Dilution Ratio | IHC 1:200-1000; WB 1:500-2000; IF 1:100-500; ELISA 1:1000-5000 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004) |
| Formulation | PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA |
| Purification | Recombinant Antibody expressed in animal component-free (ACF) media, purified via Protein G affinity chromatography. |
| Storage | -15°C to -25°C/1 year(Do not lower than -25°C) |
| Concentration | |
| Clonality | Monoclonal |
| Clone Number | RMM2242 |
| Immunogen | Synthesized peptide derived from human SALL4 AA range: 750-850 |
| Specificity | This antibody detects endogenous levels of SALL4 protein. |
| Gene Name | SALL4 ZNF797 |
| Protein Name | Sal-like protein 4 (Zinc finger protein 797) (Zinc finger protein SALL4) |
| Other Name | |
| Species | Human |
| Gene ID | 57167 |
| Uniprot | Q9UJQ4 |
| Species.1 | |
| Gene ID.1 | |
| Uniprot.1 | |
| Species.2 | |
| Gene ID.2 | |
| Uniprot.2 | |
| Cellular Localization | Nuclear |
| Tissue Expression | Expressed in testis. Constitutively expressed in acute myeloid leukemia (AML). |
| Signaling_pathway | |
| Research Areas | |
| Function | Disease:Defects in SALL4 are the cause of Duane-radial ray syndrome (DRRS) [MIM:607323]; also known as Okihiro syndrome. DRRS is a disorder characterized by the association of forearm malformations with Duane retraction syndrome.,Disease:Defects in SALL4 are the cause of IVIC syndrome [MIM:147750]. IVIC syndrome is an autosomal dominant condition characterized by upper limbs anomalies (radial ray defects, carpal bones fusion), extraocular motor disturbances, congenital bilateral non-progressive mixed hearing loss. Other less consistent malformations include heart involvement, mild thrombocytopenia and leukocytosis (before age 50), shoulder girdle hypoplasia, imperforate anus, kidney malrotation or rectovaginal fistula. The IVIC syndrome is an allelic disorder of Duane-radial ray syndrome (DRRS) with a similar phenotype.,Function:Probable transcription factor.,similarity:Belongs to the sal C2H2-type zinc-finger protein family.,similarity:Contains 7 C2H2-type zinc fingers.,subunit:Interacts with NANOG.,tissue specificity:Expressed in testis., |
