Search results for GTF2IRD1 antibody
GTF2IRD1 antibody, Genetex, GTX33232
Host
Rabbit
Reactivity
Human, Mouse, Rat
Applications
WB
Conjugation
Unconjugated
GTF2IRD1 antibody, Genetex, GTX131433
Host
Rabbit
Reactivity
Human
Applications
WB ICC/IF
Conjugation
Unconjugated
Anti-GTF2IRD1 antibody, Abcam, AB64805
Host
Rabbit
Reactivity
Human
Applications
WB
Conjugation
GTF2I Repeat Domain Containing 1 (GTF2IRD1) Antibody, Abbexa, abx328703
GTF2IRD1 Antibody is a Rabbit Polyclonal against GTF2IRD1.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Applications
ELISA, WB, IHC
Conjugation
Unconjugated
GTF2I Repeat Domain Containing 1 (GTF2IRD1) Antibody, Abbexa, abx233716
GTF2IRD1 Antibody is a Rabbit Polyclonal against GTF2IRD1.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Applications
ELISA, WB, IHC
Conjugation
Unconjugated
GTF2I Repeat Domain Containing 1 (GTF2IRD1) Antibody, Abbexa, abx030038
The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene plays a role in craniofacial and cognitive development and mutations have been associated with Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq].
Host
Rabbit
Reactivity
Human
Applications
ELISA, WB
Conjugation
Unconjugated
GTF2I Repeat Domain Containing 1 (GTF2IRD1) Antibody, Abbexa, abx005071
GTF2IRD1 Antibody is a Rabbit Polyclonal antibody against GTF2IRD1. The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene plays a role in craniofacial and cognitive development and mutations have been associated with Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing results in multiple transcript variants.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Applications
ELISA, WB
Conjugation
Unconjugated
GTF2I Repeat Domain Containing 1 (GTF2IRD1) Antibody, Abbexa, abx112869
GTF2IRD1 Antibody is a Rabbit Polyclonal antibody against GTF2IRD1.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Applications
ELISA, WB, IHC
Conjugation
Unconjugated
GTF2I Repeat Domain Containing 1 (GTF2IRD1) Antibody, Abbexa, abx013839
Rabbit polyclonal antibody against GTF2IRD1 protein. Immunogen region is N-terminal.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Applications
ELISA, WB
Conjugation
Unconjugated
GTF2I Repeat Domain Containing 1 (GTF2IRD1) Antibody, Abbexa, abx432023
GTF2IRD1 Antibody is a Goat Polyclonal antibody against GTF2IRD1.
Host
Goat
Reactivity
Human
Applications
P-ELISA, WB, IF/ICC, FCM
Conjugation
Unconjugated
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