Motor Neuron and Pancreas Homeobox 1 (MNX1) (N-Term) antibody

Details for Product No. ABIN404772
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Antigen
Synonyms HB9, HLXB9, HOXHB9, SCRA1, Hlxb9, MNR2, hlxb9, zgc:112174
Epitope
N-Term
(8), (7), (3), (2), (2), (2), (1), (1), (1), (1)
Reactivity
Mouse (Murine), Dog (Canine), Human
(29), (20), (12), (12), (12), (12), (12), (3)
Host
Rabbit
(35), (1)
Clonality
Polyclonal
Conjugate
Un-conjugated
(2), (2), (2), (1), (1), (1), (1), (1), (1), (1), (1), (1), (1), (1)
Application
Western Blotting (WB)
(20), (10), (9), (4), (3), (1), (1), (1), (1)
Pubmed 1 reference available
Quantity 50 µg
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Catalog No. ABIN404772
289.00 $
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Immunogen Synthetic peptide directed towards the N terminal of human MNX1
Sequence AAASGTGGGG GGGGASGGTS GSCSPASSEP PAAPADRLRA ESPSPPRLLA
Predicted Reactivity Human : 100 %, Pig : 90 %, Dog : 80 %, Mouse : 70 %
Characteristics This is a rabbit polyclonal antibody against MNX1. It was validated on Western Blot using a cell lysate as a positive control.
Purification Affinity Purified
Alternative Name MNX1
Background MNX1 contains 1 homeobox DNA-binding domain. MNX1 is a putative transcription factor involved in pancreas development and function. Defects in MNX1 are a cause of Currarino syndrome.
Molecular Weight 40 kDa
Gene ID 3110
NCBI Accession NP_005506, NM_005515
UniProt P50219
Application Notes Optimal working dilutions should be determined experimentally by the investigator.
Comment

Antigen size: 401 AA

Restrictions For Research Use only
Format Lyophilized
Reconstitution Add 50 µL of distilled water.
Concentration 1 mg/mL
Buffer PBS buffer with 2 % sucrose
Handling Advice Avoid repeated freeze-thaw cycles.
Storage -20 °C
Storage Comment For longer periods of storage, store at -20 °C
Supplier Images
anti-Motor Neuron and Pancreas Homeobox 1 (MNX1) (N-Term) antibody WB Suggested Anti-MNX1 Antibody Titration: 0.2-1 ug/ml
ELISA Titer: 1:62500
Positive Control: HepG2 cell lysate
Background publications Kim, Oh, Choi et al.: "Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome." in: Journal of human genetics, Vol. 52, Issue 8, pp. 698-701, 2007 (PubMed).

Validation Images
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