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Rabbit Anti-MNX1 (C-terminus) Recombinant Antibody (CBFYM-2444) (CBMAB-M2631-FY)

This product is rabbit antibody that recognizes MNX1. The antibody CBFYM-2444 can be used for immunoassay techniques such as: WB, IP, IHC-P.
See all MNX1 antibodies

Summary

Host Animal
Rabbit
Specificity
Mouse, Human
Clone
CBFYM-2444
Antibody Isotype
IgG
Application
WB, IP, IHC-P

Basic Information

Immunogen
A synthetic peptide corresponding to residues near the C-terminus of human HB9
Specificity
Mouse, Human
Antibody Isotype
IgG
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS, 0.05% BSA, 50% glycerol
Preservative
0.01% Sodium azide
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.
Epitope
C-terminus

Target

Full Name
MOTOR NEURON AND PANCREAS HOMEOBOX 1
Introduction
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.
Entrez Gene ID
Human3110
Mouse15285
UniProt ID
HumanP50219
MouseQ9QZW9
Alternative Names
Motor Neuron And Pancreas Homeobox 1; Homeobox Protein HB9; Homeobox HB9; HLXB9; Motor Neuron And Pancreas Homeobox Protein 1; Homeo Box HB9; HOXHB9; SCRA1; HB9
Function
Putative transcription factor involved in pancreas development and function.
Biological Process
Central nervous system development Source: GO_Central
Endocrine pancreas development Source: GO_Central
Neuron projection morphogenesis Source: GO_Central
Spinal cord motor neuron cell fate specification Source: GO_Central
Cellular Location
Nucleus
Involvement in disease
Currarino syndrome (CURRAS):
The triad of a presacral tumor, sacral agenesis and anorectal malformation constitutes the Currarino syndrome which is caused by dorsal-ventral patterning defects during embryonic development. The syndrome occurs in the majority of patients as an autosomal dominant trait.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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