BBS4 polyclonal antibody

Catalog # PAB18993

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Price

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Quantity

Size:100 ug
Price: USD $ 428.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot (Cell lysate)
Application

Western Blot (Cell lysate)

BBS4 polyclonal antibody (Cat # PAB18993, 1 ug/mL) staining of HeLa lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.

  • Specification

    Product Description

    Goat polyclonal antibody raised against synthetic peptide of BBS4.

    Immunogen

    A synthetic peptide corresponding to amino acids at internal region of human BBS4.

    Sequence

    C-NEAAKLNQKDWEISH

    Host

    Goat

    Theoretical MW (kDa)

    60

    Reactivity

    Human

    Form

    Liquid

    Purification

    Antigen affinity purification

    Concentration

    0.5 mg/mL

    Recommend Usage

    ELISA (1:32000)
    Western Blot (1-3 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In 0.5 mg/mL in Tris saline, pH7.3 (0.5% BSA, 0.02% sodium azide)

    Storage Instruction

    Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Western Blot (Cell lysate)

    BBS4 polyclonal antibody (Cat # PAB18993, 1 ug/mL) staining of HeLa lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — BBS4

    Entrez GeneID

    585

    Protein Accession#

    NP_149017.2

    Gene Name

    BBS4

    Gene Alias

    -

    Gene Description

    Bardet-Biedl syndrome 4

    Omim ID

    209900 600374

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse. The similar phenotypes exhibited by mutations in BBS gene family members are likely due to the protein's shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene has sequence similarity to O-linked N-acetylglucosamine (O-GlcNAc) transferases in plants and archaebacteria and in human forms a multi-protein "BBSome" complex with six other BBS proteins. Alternative splice variants have been described but their predicted protein products have not been experimentally verified

    Other Designations

    -

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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