DFNA5/GSDME Polyclonal antibody
DFNA5/GSDME Polyclonal Antibody for WB, ELISA
Host / Isotype
Rabbit / IgG
Reactivity
mouse
Applications
WB, ELISA
Conjugate
Unconjugated
Cat no : 30696-1-AP
Synonyms
Validation Data Gallery
Tested Applications
Positive WB detected in | J774A.1 cells, mouse brain tissue, rat brain tissue |
Recommended dilution
Application | Dilution |
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Western Blot (WB) | WB : 1:500-1:2000 |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
Product Information
30696-1-AP targets DFNA5/GSDME in WB, ELISA applications and shows reactivity with mouse samples.
Tested Reactivity | mouse |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Type | Antibody |
Immunogen | DFNA5/GSDME fusion protein Ag33622 相同性解析による交差性が予測される生物種 |
Full Name | deafness, autosomal dominant 5 (human) |
Calculated molecular weight | 57 kDa |
Observed molecular weight | 57 kDa |
GenBank accession number | BC132303 |
Gene symbol | DFNA5/GSDME |
Gene ID (NCBI) | 54722 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Antigen affinity purification |
Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
Background Information
DFNA5 (deafness, autosomal dominant 5), also known as GSDME or ICERE-1, is a 496 amino acid protein that is expressed in cochlea tissue, as well as in placenta, brain, heart, liver, lung and pancreas. Defects in the gene encoding DFNA5 are the cause of non-syndromic sensorineural deafness autosomal dominant type 5 (DFNA5), a form of sensorineural hearing loss that results from damage to one of various structures that receive sound information in the brain.
Protocols
Product Specific Protocols | |
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WB protocol for DFNA5/GSDME antibody 30696-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |