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BCL7B antibody
BCL7B
Reactivity: Human, Mouse
ELISA, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-BCL7B Antibody
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Target
See all BCL7B Antibodies
BCL7B
(B-Cell CLL/lymphoma 7B (BCL7B))
Reactivity
All reactivities for BCL7B antibodies
Human, Mouse
Host
All hosts for BCL7B antibodies
Rabbit
Clonality
All clonalities for BCL7B antibodies
Polyclonal
Conjugate
All conjugates for BCL7B antibodies
This BCL7B antibody is un-conjugated
Application
All applications for BCL7B antibodies
ELISA, Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Antigen affinity purification
Immunogen
Fusion protein of human BCL7B
Isotype
IgG
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Discover our top product BCL7B Primary Antibody
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Application Details
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Application Notes
IHC 1:50-1:200, ELISA 1:5000-1:10000
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
1.5 mg/mL
Buffer
PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for BCL7B
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Target
BCL7B
(B-Cell CLL/lymphoma 7B (BCL7B))
Alternative Name
BCL7B (BCL7B Products )
Synonyms
bcl7b antibody, zgc:103501 antibody, wu:fb94h01 antibody, zgc:85678 antibody, B-cell CLL/lymphoma 7B, b antibody, B-cell CLL/lymphoma 7B, a antibody, B-cell CLL/lymphoma 7B antibody, B-cell CLL/lymphoma 7b antibody, B cell CLL/lymphoma 7B antibody, BCL tumor suppressor 7B antibody, bcl7bb antibody, bcl7ba antibody, bcl7b antibody, Bcl7b antibody, BCL7B antibody
Background
This gene encodes a member of the BCL7 family including BCL7A, BCL7B and BCL7C proteins. This member is BCL7B, which contains a region that is highly similar to the N-terminal segment of BCL7A or BCL7C proteins. The BCL7A protein is encoded by the gene known to be directly involved in a three-way gene translocation in a Burkitt lymphoma cell line. This gene is located at a chromosomal region commonly deleted in Williams syndrome. This gene is highly conserved from C. elegans to human. Multiple alternatively spliced transcript variants have been found for this gene.
UniProt
Q9BQE9
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