AHI1 Antibody - BSA Free

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Immunocytochemistry/ Immunofluorescence: AHI1 Antibody [NBP2-55373] - Staining of human cell line SiHa shows localization to centrosome.

Product Details

Summary
Reactivity HuSpecies Glossary
Applications ICC/IF
Clonality
Polyclonal
Host
Rabbit
Conjugate
Unconjugated
Format
BSA Free

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Catalog# & Formulation Size Price

AHI1 Antibody - BSA Free Summary

Description
Novus Biologicals Rabbit AHI1 Antibody - BSA Free (NBP2-55373) is a polyclonal antibody validated for use in ICC/IF. All Novus Biologicals antibodies are covered by our 100% guarantee.
Immunogen
This antibody was developed against a recombinant protein corresponding to the following amino acid sequence: QVAMYSDLPFKSPIRDISYHPFENMVAFCAFGQNEPILLYIYDFHVAQQEAEMFKRYNGTFPLPGIHQSQDALCTCPKLPHQGSFQIDEFVHTESSSTKMQLVKQ
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
AHI1
Purity
Affinity purified
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Applications/Dilutions

Dilutions
  • Immunocytochemistry/ Immunofluorescence 0.25-2 ug/ml
Application Notes
ICC/IF,,Fixation Permeabilization: Use PFA/Triton X-100.
Control Peptide
AHI1 Recombinant Protein Antigen (NBP2-55373PEP)

Reactivity Notes

Mouse 88%, Rat 87%

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
PBS (pH 7.2) and 40% Glycerol
Preservative
0.02% Sodium Azide
Purity
Affinity purified

Alternate Names for AHI1 Antibody - BSA Free

  • Abelson helper integration site 1 protein homolog
  • Abelson helper integration site 1
  • Abelson helper integration site
  • AHI-1
  • contatins SH3 and WD40 domains
  • dJ71N10.1
  • DKFZp686J1653
  • FLJ14023
  • FLJ20069
  • JBTS3
  • jouberin
  • ORF1

Background

Jouberin (AHI1), encoding the Jouberin protein, is an alternatively spliced signaling molecule that contains seven Trp-Asp (WD) repeats, an SH3 domain, and numerous SH3-binding sites. The gene is expressed strongly in embryonic hindbrain and forebrain, and AHI1 may be required for both cerebellar and cortical development in humans. Defects in AHI1 are the cause of Joubert syndrome 3, an autosomal recessive brain congenital malformation. The exact function of the AHI1 gene is not yet known.

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

ICC/IF Video Protocol

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Bioinformatics

Gene Symbol AHI1