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The antibody against MNX1 was raised in rabbit using the Recombinant Human Motor neuron and pancreas homeobox protein 1 protein (50-99AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB.
The antibody against MNX1 was raised in rabbit using the Recombinant Human Motor neuron and pancreas homeobox protein 1 protein (50-99AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB.
$299.00
| Cat.No | ADC-08896A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | MNX1 |
| Form | Liquid | Species Reactivity | Human |
| Isotype | IgG | Storage Buffer | 0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4 |
| Purification Method | >95%, Protein G purified | Conjugate | Non-conjugated |
| Application | ELISA, WB | Storage | Upon receipt |
| Immunogen Description | Recombinant Human Motor neuron and pancreas homeobox protein 1 protein (50-99AA) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | P50219 |
Uniprot Id
P50219
Target Species
Human
Target Name
MNX1
Target Full Name
Motor neuron and pancreas homeobox protein 1
Target Function
Putative transcription factor involved in pancreas development and function.
Target Involvement
Currarino syndrome (CURRAS)
Target Subcellular Location
Nucleus.
Target Tissue Specificity
Expressed in lymphoid and pancreatic tissues.
Target Synonyms
HB 9; HB9; HLXB 9; HLXB9; Homeo box HB9; Homeobox HB9; Homeobox protein HB9; HOXHB9; MNX1; MNX1_HUMAN; Motor neuron and pancreas homeobox 1; Motor neuron and pancreas homeobox protein 1; Sacral agenesis autosomal dominant (Currarino triad); SCRA 1; SCRA1
Target Background
This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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