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Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting immunostaining in relation to complex human pathologies.

Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding. Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".

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CCDC85B Antibody (aa69‑96) LS‑C167419 Best Seller
CCDC85B antibody LS-C167419 is an unconjugated rabbit polyclonal antibody to human CCDC85B. Validated for Flow, IHC and WB.
Catalog
Size
Price
LS-C167419-400
400 µl
$305

Popular CCDC85B Products

Antibody
Species: Human
Applications: Western blot, ELISA
CCDC85B antibody Western blot of COL0205 Cell lysate. Antibody concentration 1 ug/ml.  This image was taken for the unconjugated form of this product. Other forms have not been tested.
Species: Human, Monkey, Mouse, Rat, Bovine, Dog, Guinea pig, Hamster, Pig, Zebrafish
Applications: Western blot
CCDC85B antibody Western blot of COL0205 Cell lysate. Antibody concentration 1 ug/ml.  This image was taken for the unconjugated form of this product. Other forms have not been tested.
Species: Human, Chimpanzee, Monkey, Mouse, Rat, Bovine, Dog, Guinea pig, Hamster, Pig, Zebrafish
Applications: Western blot
CCDC85B antibody Western blot of COL0205 Cell lysate. Antibody concentration 1 ug/ml.  This image was taken for the unconjugated form of this product. Other forms have not been tested.
Species: Human, Chimpanzee, Monkey, Mouse, Rat, Bovine, Dog, Guinea pig, Hamster, Pig, Zebrafish
Applications: Western blot

Product Description

CCDC85B antibody LS-C167419 is an unconjugated rabbit polyclonal antibody to human CCDC85B. Validated for Flow, IHC and WB.

Specifications

Target
Human CCDC85B
Synonyms
CCDC85B, Delta-interacting protein A, DIPA
Host
Rabbit
Reactivity
Human (tested or 100% immunogen sequence identity)
Predicted
Mouse (at least 90% immunogen sequence identity)
Clonality
Polyclonal
Conjugations
Unconjugated
Purification
Ammonium sulfate precipitation
Modifications
Unmodified
Applications
  • IHC
  • IHC - Paraffin (1:50 - 1:100)
  • Western blot (1:1000)
  • Flow Cytometry (1:10 - 1:50)
Performing IHC? See our complete line of Immunohistochemistry Reagents including antigen retrieval solutions, blocking agents ABC Detection Kits and polymers, biotinylated secondary antibodies, substrates and more.
Blocking Peptide
LS-E9949 - Lyophilized - 100 µg - $145.00
Immunizing peptide used to generate LS-C167419. Useful for pre-absorption and neutralization of the antibody's antigen binding site.
Epitope
aa69-96
Specificity
This DIPA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 69-96 amino acids from the Central region of human DIPA.
Presentation
PBS, 0.09% Sodium Azide
Storage
Maintain refrigerated at 2°C to 8°C for up to 6 months. For long term storage store at -20°C.
Restrictions
For research use only.
About CCDC85B
Hepatitis delta virus (HDV) is a pathogenic human virus whose RNA genome and replication cycle resemble those of plant viroids. Delta-interacting protein A (DIPA), a cellular gene product, has been found to have homology to hepatitis delta virus antigen (HDAg). DIPA interacts with the viral antigen, HDAg, and can affect HDV replication in vitro. Q15834 NM_006848 NP_006839.2


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Images

Immunohistochemistry

Formalin-fixed and paraffin-embedded human skeletal muscle reacted with DIPA Antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.
Formalin-fixed and paraffin-embedded human skeletal muscle reacted with DIPA Antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.

Western blot

Western blot of DIPA Antibody in HepG2 cell line lysates (35 ug/lane). DIPA (arrow) was detected using the purified antibody.
Western blot of DIPA Antibody in HepG2 cell line lysates (35 ug/lane). DIPA (arrow) was detected using the purified antibody.

Flow Cytometry

DIPA Antibody flow cytometry of HepG2 cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
DIPA Antibody flow cytometry of HepG2 cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Immunohistochemistry

Formalin-fixed and paraffin-embedded human skeletal muscle reacted with DIPA Antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.
Formalin-fixed and paraffin-embedded human skeletal muscle reacted with DIPA Antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.

Western blot

Western blot of DIPA Antibody in HepG2 cell line lysates (35 ug/lane). DIPA (arrow) was detected using the purified antibody.
Western blot of DIPA Antibody in HepG2 cell line lysates (35 ug/lane). DIPA (arrow) was detected using the purified antibody.

Flow Cytometry

DIPA Antibody flow cytometry of HepG2 cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
DIPA Antibody flow cytometry of HepG2 cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Immunohistochemistry

Formalin-fixed and paraffin-embedded human skeletal muscle reacted with DIPA Antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.
Formalin-fixed and paraffin-embedded human skeletal muscle reacted with DIPA Antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.

Western blot

Western blot of DIPA Antibody in HepG2 cell line lysates (35 ug/lane). DIPA (arrow) was detected using the purified antibody.
Western blot of DIPA Antibody in HepG2 cell line lysates (35 ug/lane). DIPA (arrow) was detected using the purified antibody.

Flow Cytometry

DIPA Antibody flow cytometry of HepG2 cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
DIPA Antibody flow cytometry of HepG2 cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Immunohistochemistry

Formalin-fixed and paraffin-embedded human skeletal muscle reacted with DIPA Antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.
Formalin-fixed and paraffin-embedded human skeletal muscle reacted with DIPA Antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.

Western blot

Western blot of DIPA Antibody in HepG2 cell line lysates (35 ug/lane). DIPA (arrow) was detected using the purified antibody.
Western blot of DIPA Antibody in HepG2 cell line lysates (35 ug/lane). DIPA (arrow) was detected using the purified antibody.

Flow Cytometry

DIPA Antibody flow cytometry of HepG2 cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
DIPA Antibody flow cytometry of HepG2 cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Requested From: United States
Date Requested: 11/14/2018

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