Rabbit Polyclonal Anti-Tubulin gamma antibody (STJ98974)


Reactivity: Human, Mouse, Rat
Applications: WB, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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Rabbit Polyclonal Anti-Tubulin gamma antibody (STJ98974)

Supplier: St John’s Laboratory Ltd.

Recommended applications: WB, ELISA

Recommended dilution: WB 1:500-2000; ELISA 1:10000-20000

Recommended protocols: check protocols

Image descriptions:

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Alternative names:

Check alternative names for the antibody


|Gamma-1-tubulin antibody|Gamma-tubulin complex component 1 antibody|GCP-1 antibody|TBG1_HUMAN antibody|TUBG antibody|TUBG1 antibody|TUBGCP1 antibody|Tubulin gamma-1 chain antibody|Tubulin, gamma 1 antibody|Tubulin, gamma polypeptide antibody|Anti-TUBG1 antibody [EPR8449] (ab129021)
SCBT cat No:


Anti-Tubulin gamma antibody

Catalogue No.



Human, Mouse, Rat


Anti-Tubulin gamma antibody detects endogenous Tubulin gamma .


Synthetic peptide from human protein at AA range: 380-440.












Anti-Tubulin gamma antibody was tube-contained in liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.


1 mg/ml


Anti-Tubulin gamma antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.


-20 Celsius degree. Avoid repeated freeze/thaw cycles.

Alternative antibody names

Gamma-1-tubulin antibody, Gamma-tubulin complex component 1 antibody, GCP-1 antibody, TBG1_HUMAN antibody, TUBG antibody, TUBG1 antibody, TUBGCP1 antibody, Tubulin gamma-1 chain antibody, Tubulin, gamma 1 antibody, Tubulin, gamma polypeptide antibody

Protein function

Tubulin is the major constituent of microtubules. The gamma chain is found at microtubule organizing centers (MTOC) such as the spindle poles or the centrosome. Pericentriolar matrix component that regulates alpha/beta chain minus-end nucleation, centrosome duplication and spindle formation.

Involvement in disease

Cortical dysplasia, complex, with other brain malformations 4 (CDCBM4) [MIM:615412]: A disorder of aberrant neuronal migration and disturbed axonal guidance. Clinical features include early-onset seizures, microcephaly, spastic tetraplegia, and various malformations of cortical development, such as agyria, posterior or frontal pachygyria, thick cortex, and subcortical band heterotopia and thin corpus callosum in some patients. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the tubulin family.

Protein post-translational modifications

Phosphorylation at Ser-131 by BRSK1 regulates centrosome duplication, possibly by mediating relocation of gamma-tubulin and its associated proteins from the cytoplasm to the centrosome. .

Protein cellular localization

Cytoplasm, cytoskeleton, microtubule organizing center, centrosome .


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St John’s Laboratory Ltd.

Product type

Primary antibody


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