ARG63586

anti-MSX1 antibody

anti-MSX1 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human

Developmental Biology antibody; Gene Regulation antibody; Neuroscience antibody

Overview

Product Description Goat Polyclonal antibody recognizes MSX1
Tested Reactivity Hu
Predict Reactivity Ms, Rat, Cow, Pig
Tested Application IHC-P, WB
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name MSX1
Antigen Species Human
Immunogen TSLPLGVKVEDS-C
Conjugation Un-conjugated
Alternate Names HYD1; Msh homeobox 1-like protein; HOX7; Homeobox protein Hox-7; Homeobox protein MSX-1; ECTD3; STHAG1

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P2 - 4 µg/ml
WB1 µg/ml
Application Note IHC-P: Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0).
WB: Recommend incubate at RT for 1h.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purified from goat serum by antigen affinity chromatography.
Buffer Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA.
Preservative 0.02% Sodium azide
Stabilizer 0.5% BSA
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 4487 Human MSX1

Swiss-port # P28360 Human Homeobox protein MSX-1

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. [provided by RefSeq, Jul 2008]
Research Area Developmental Biology antibody; Gene Regulation antibody; Neuroscience antibody
Calculated MW 31 kDa
PTM Sumoylated by PIAS1, desumoylated by SENP1.