ARG45218

anti-GRHL2 antibody

anti-GRHL2 antibody for Flow cytometry,ICC/IF,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human

Overview

Product Description Rabbit Polyclonal antibody recognizes GRHL2
Tested Reactivity Hu
Tested Application FACS, ICC/IF, IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name GRHL2
Antigen Species Human
Immunogen Recombinant protein containing to human GRHL2.
Conjugation Un-conjugated
Alternate Names GRHL2; Grainyhead Like Transcription Factor 2; BOM; Transcription Factor CP2-Like 3; TFCP2L3; Grainyhead-Like Protein 2 Homolog; Brother Of Mammalian Grainyhead; Brother-Of-MGR; FLJ13782; DFNA28; Deafness, Autosomal Dominant 28; Grainyhead-Like 2 (Drosophila); Grainyhead-Like 2; ECTDS; PPCD4

Application Instructions

Application Suggestion
Tested Application Dilution
FACS1 - 3 µg/10^6 cells
ICC/IF5 μg/ml
IHC-P2-5 μg/ml
WB0.25-0.5 μg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size 71 kDa

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer 0.2% Na2HPO4, 0.9% NaCl and 4% Trehalose.
Stabilizer 4% Trehalose
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: 79977 Human GRHL2

Swiss-port # Q6ISB3 Human Grainyhead-like protein 2 homolog

Gene Symbol GRHL2
Gene Full Name Grainyhead Like Transcription Factor 2
Background The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).[provided by RefSeq, Mar 2009]
Function Transcription factor playing an important role in primary neurulation and in epithelial development. [UniProt]
Cellular Localization Membrane; Nucleus [UniProt]
Calculated MW 71 kDa