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MNX1 antibody (Middle Region)
MNX1
Reactivity: Human, Mouse
WB, EIA
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-MNX1 Antibody
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Target
See all MNX1 Antibodies
MNX1
(Motor Neuron and Pancreas Homeobox 1 (MNX1))
Binding Specificity
All epitopes for MNX1 antibodies
AA 241-271, Middle Region
Reactivity
All reactivities for MNX1 antibodies
Human, Mouse
Host
All hosts for MNX1 antibodies
Rabbit
Clonality
All clonalities for MNX1 antibodies
Polyclonal
Conjugate
All conjugates for MNX1 antibodies
This MNX1 antibody is un-conjugated
Application
All applications for MNX1 antibodies
Western Blotting (WB), Enzyme Immunoassay (EIA)
Specificity
This antibody recognizes Human and Mouse MNX1 (Center).
Purification
Protein A column, followed by peptide affinity purification
Immunogen
KLH conjugated synthetic peptide between 241-271 amino acids from the Central region of human MNX1
Isotype
Ig Fraction
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Discover our top product MNX1 Primary Antibody
Alternatives
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Application Details
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Application Notes
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.25 mg/mL
Buffer
PBS containing 0.09 % (W/V) Sodium Azide as preservative
Preservative
Sodium azide
Precaution of Use
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handling Advice
Avoid repeated freezing and thawing.
Storage
4 °C/-20 °C
Storage Comment
Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
Target Details for MNX1
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Target
MNX1
(Motor Neuron and Pancreas Homeobox 1 (MNX1))
Alternative Name
MNX1 (MNX1 Products )
Synonyms
HB9 antibody, HLXB9 antibody, HOXHB9 antibody, SCRA1 antibody, Hlxb9 antibody, MNR2 antibody, hlxb9 antibody, zgc:112174 antibody, motor neuron and pancreas homeobox 1 antibody, motor neuron homeobox transcription factor antibody, MNX1 antibody, mnx1 antibody, Mnx1 antibody
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. [provided by RefSeq].Synonyms: HLXB9, Homeobox protein HB9, Motor neuron and pancreas homeobox protein 1
Molecular Weight
40569 Da
Gene ID
3110
NCBI Accession
NP_005506
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