MSX1 antibody (AA 111-138)

Catalog No. ABIN1537757

The Rabbit Polyclonal anti-MSX1 antibody has been validated for WB and IF. It is suitable to detect MSX1 in samples from Human and Mouse.

Quick Overview for MSX1 antibody (AA 111-138) (ABIN1537757)

Target: MSX1 (Msh Homeobox 1 (MSX1))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MSX1 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Clone: RB30384

Product Details anti-MSX1 Antibody

Binding Specificity: AA 111-138

Predicted Reactivity: B

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

Immunogen: This MSX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 111-138 amino acids from the Central region of human MSX1.

Isotype: Ig Fraction

Application Details

Application Notes: IF: 1:10~50. IF: 1:200. WB: 1:1000. WB: 1:2000. WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody 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: MSX1 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Expiry Date: 6 months

Target Details for MSX1

Target: MSX1 (Msh Homeobox 1 (MSX1))

Alternative Name: MSX1

Background: This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia.

Molecular Weight: 31496

Gene ID: 4487

NCBI Accession: NP_002439

UniProt: P28360

Pathways: Regulation of Muscle Cell Differentiation, Positive Regulation of Response to DNA Damage Stimulus