COG4 Antibody

Code CSB-PA881003ESR2HU
Size US$166
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  • Western blot
    All lanes: COG4 antibody at 4.85µg/ml
    Lane 1: Mouse liver tissue
    Lane 2: Mouse gonadal tissue
    Lane 3: K562 whole cell lysate
    Lane 4: Hela whole cell lysate
    Secondary
    Goat polyclonal to rabbit IgG at 1/10000 dilution
    Predicted band size: 90, 39, 82 kDa
    Observed band size: 90 kDa

  • Immunohistochemistry of paraffin-embedded human tonsil tissue using CSB-PA881003ESR2HU at dilution of 1:100

  • Immunohistochemistry of paraffin-embedded human kidney tissue using CSB-PA881003ESR2HU at dilution of 1:100

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) COG4 Polyclonal antibody
Uniprot No.
Target Names
COG4
Alternative Names
COG4Conserved oligomeric Golgi complex subunit 4 antibody; COG complex subunit 4 antibody; Component of oligomeric Golgi complex 4 antibody
Raised in
Rabbit
Species Reactivity
Human, Mouse
Immunogen
Recombinant Human Conserved oligomeric Golgi complex subunit 4 protein (506-785AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Form
Liquid
Tested Applications
ELISA, WB, IHC
Recommended Dilution
Application Recommended Dilution
WB 1:1000-1:5000
IHC 1:20-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Function
Required for normal Golgi function. Plays a role in SNARE-pin assembly and Golgi-to-ER retrograde transport via its interaction with SCFD1.
Gene References into Functions
  1. A novel R729W missense mutation in COG4 was associated with the congenital disorder of glycosylation type II. PMID: 19494034
  2. The 1.9 A crystal structure of a Cog4 C-terminal fragment, was determined. Arg 729 is found to occupy a key position at the center of a salt bridge network, thereby stabilizing Cog4's small C-terminal domain. PMID: 19651599
Involvement in disease
Congenital disorder of glycosylation 2J (CDG2J)
Subcellular Location
Cytoplasm, cytosol. Golgi apparatus membrane; Peripheral membrane protein; Cytoplasmic side.
Protein Families
COG4 family
Database Links

HGNC: 18620

OMIM: 606976

KEGG: hsa:25839

STRING: 9606.ENSP00000315775

UniGene: Hs.208680

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