Recombinatie DFNA5 / GSDME monoklonaal antilichaam

Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.

DFNA5

O60443

Human; Mouse; Rat

Recombinant Human DFNA5/GSDME protein

DFNA; DFNA5; ICERE-1; GSDME; ICERE1;2310037D07Rik;4932441K13Rik; autosomal dominant 5; autosomal dominant 5 protein; Deafness; DFNA5 gene; Dfna5h; EG14210; Fin15; ICERE 1; Inversely correlated with estrogen receptor expression 1; Nonsyndromic hearing impairment protein; Non-syndromic hearing impairment protein 5; DFNA5

3G8

Unconjugated

WB

Neuroscience

Protein A

0.2 mg/mL

WB 1:2000-1:10000

PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.

Ice bag

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

https://789.bio/eb/TM2JlyO9

55 kDa

55 kDa

IgG, κ