Dfna5 Antibody - BSA Free

Images

 
Immunohistochemistry: Dfna5 Antibody - BSA Free [NBP3-48021] - Immunohistochemistry of paraffin-embedded human brain using (Dfna5 antibody) at dilution of 1:100
Western Blot: Dfna5 Antibody - BSA Free [NBP3-48021] - Mouse lung tissue were subjected to SDS PAGE followed by western blot with (Dfna5 antibody) at dilution of 1:1000

Product Details

Summary
Reactivity Hu, Mu, RtSpecies Glossary
Applications WB, ELISA, IHC
Clonality
Polyclonal
Host
Rabbit
Conjugate
Unconjugated
Format
BSA Free

Order Details

Dfna5 Antibody - BSA Free Summary

Description
Novus Biologicals Rabbit Dfna5 Antibody - BSA Free (NBP3-48021) is a polyclonal antibody validated for use in IHC, WB and ELISA. All Novus Biologicals antibodies are covered by our 100% guarantee.
Immunogen
deafness, autosomal dominant 5. (Uniprot# O60443)
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
GSDME
Purity
Immunogen affinity purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • ELISA
  • Immunohistochemistry 1:50 - 1:200
  • Western Blot 1:500 - 1:2000
Theoretical MW
54 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

Storage
Store at -20C. Avoid freeze-thaw cycles.
Buffer
PBS, 50% Glycerol, pH (7.3)
Preservative
0.02% Sodium Azide
Purity
Immunogen affinity purified

Alternate Names for Dfna5 Antibody - BSA Free

  • deafness, autosomal dominant 5
  • DFNA5, deafness associated tumor suppressor
  • gasdermin-E
  • ICERE1
  • ICERE-1
  • Inversely correlated with estrogen receptor expression 1
  • non-syndromic hearing impairment protein 5
  • nonsyndromic hearing impairment protein

Background

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. [provided by RefSeq]

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Product General Protocols

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Video Protocols

WB Video Protocol

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Secondary Antibodies

 

Isotype Controls

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Bioinformatics

Gene Symbol GSDME