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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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RCBTB2 Antibody (aa71‑99) LS‑C168722
RCBTB2 antibody LS-C168722 is an unconjugated rabbit polyclonal antibody to RCBTB2 from human and mouse. Validated for Flow, IHC and WB.
Catalog
Size
Price
LS-C168722-400
400 µl
Unavailable

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Product Description

RCBTB2 antibody LS-C168722 is an unconjugated rabbit polyclonal antibody to RCBTB2 from human and mouse. Validated for Flow, IHC and WB.
About RCBTB2
RCBTB2 encodes a protein containing two C-terminal BTB/POZ domains that is related to regulator of chromosome condensation (RCC). The encoded protein may act as a guanine nucleotide exchange factor. This gene is observed to be lost or underexpressed in prostate cancers. There is a pseudogene of this gene on chromosome 10. Alternative splicing results in multiple transcript variants. O95199 NM_001268 NP_001259.1

RCBTB2 Antibody, Chromosome condensation 1-like Antibody, CHC1-L Antibody, RCC1-like G exchanging factor Antibody, RLG Antibody, CHC1L Antibody


Specifications

Target
Human RCBTB2
Host
Rabbit
Reactivity
Human, Mouse (tested or 100% 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-E8431 - Lyophilized - 100 µg - $145.00
Immunizing peptide used to generate LS-C168722. Useful for pre-absorption and neutralization of the antibody's antigen binding site.
Epitope
aa71-99
Specificity
This CHC1L antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 71-99 amino acids from the N-terminal region of human CHC1L.
Presentation
PBS, 0.09% sodium azide
Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
Restrictions
For research use only.
Guarantee
This antibody carries the LSBio 100% Guarantee.

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Customer Reviews (0)


Images


Immunohistochemistry

Formalin-fixed and paraffin-embedded human brain tissue reacted with CHC1L 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 brain tissue reacted with CHC1L 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 CHC1L Antibody in mouse thymus tissue lysates (35 ug/lane). CHC1L (arrow) was detected using the purified antibody.
Western blot of CHC1L Antibody in mouse thymus tissue lysates (35 ug/lane). CHC1L (arrow) was detected using the purified antibody.

Flow Cytometry

CHC1L Antibody flow cytometry of Jurkat cells (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
CHC1L Antibody flow cytometry of Jurkat cells (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Immunohistochemistry

Formalin-fixed and paraffin-embedded human brain tissue reacted with CHC1L 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 brain tissue reacted with CHC1L 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 CHC1L Antibody in mouse thymus tissue lysates (35 ug/lane). CHC1L (arrow) was detected using the purified antibody.
Western blot of CHC1L Antibody in mouse thymus tissue lysates (35 ug/lane). CHC1L (arrow) was detected using the purified antibody.

Flow Cytometry

CHC1L Antibody flow cytometry of Jurkat cells (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
CHC1L Antibody flow cytometry of Jurkat cells (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Immunohistochemistry

Formalin-fixed and paraffin-embedded human brain tissue reacted with CHC1L 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 brain tissue reacted with CHC1L 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 CHC1L Antibody in mouse thymus tissue lysates (35 ug/lane). CHC1L (arrow) was detected using the purified antibody.
Western blot of CHC1L Antibody in mouse thymus tissue lysates (35 ug/lane). CHC1L (arrow) was detected using the purified antibody.

Flow Cytometry

CHC1L Antibody flow cytometry of Jurkat cells (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
CHC1L Antibody flow cytometry of Jurkat cells (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

Immunohistochemistry

Formalin-fixed and paraffin-embedded human brain tissue reacted with CHC1L 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 brain tissue reacted with CHC1L 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 CHC1L Antibody in mouse thymus tissue lysates (35 ug/lane). CHC1L (arrow) was detected using the purified antibody.
Western blot of CHC1L Antibody in mouse thymus tissue lysates (35 ug/lane). CHC1L (arrow) was detected using the purified antibody.

Flow Cytometry

CHC1L Antibody flow cytometry of Jurkat cells (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
CHC1L Antibody flow cytometry of Jurkat cells (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.


Requested From: 
Date Requested: 6/20/2018

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