MNX1 antibody (AA 242-271)

Catalog No. ABIN5535259

Product Details anti-MNX1 Antibody

Target: MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))

Binding Specificity: AA 242-271

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MNX1 antibody is un-conjugated

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This MNX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 242-271 amino acids from the Central region of human MNX1.

Isotype: Ig Fraction

Application Details

Application Notes: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Target Details for MNX1

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].

Molecular Weight: 41 kDa

Gene ID: 3110

UniProt: P50219