Validation Data Gallery
|Positive WB detected in||human placenta tissue, mouse lung tissue|
|Positive IP detected in||mouse lung tissue|
|Positive IHC detected in||human testis tissue, human colon tissue|
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
|Positive IF detected in||HepG2 cells|
|Positive FC detected in||HepG2 cells|
|Western Blot (WB)||WB : 1:200-1:1000|
|Immunoprecipitation (IP)||IP : 0.5-4.0 ug for IP and 1:200-1:1000 for WB|
|Immunohistochemistry (IHC)||IHC : 1:20-1:200|
|Immunofluorescence (IF)||IF : 1:10-1:100|
|Sample-dependent, check data in validation data gallery|
19949-1-AP targets GLI3-Specific in WB, IP, IHC, IF, FC, ELISA applications and shows reactivity with human, mouse, rat samples.
|Tested Reactivity||human, mouse, rat|
|Cited Reactivity||human, mouse|
|Host / Isotype||Rabbit / IgG|
|Full Name||GLI family zinc finger 3|
|Calculated molecular weight||170 kDa|
|Observed molecular weight||190 kDa, 83-86 kDa|
|GenBank accession number||NM_000168|
|Gene ID (NCBI)||2737|
|Purification Method||Antigen affinity purification|
|Storage Buffer||PBS with 0.02% sodium azide and 50% glycerol pH 7.3.|
|Storage Conditions||Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.|
GLI3 belongs to the GLI C2H2-type zinc-finger protein family. GLI3 plays a role in limb and brain development. GLI3 is implicated in the transduction of SHH signal. Defects in GLI3 are the cause of Greig cephalo-poly-syndactyly syndrome (GCPS). Defects in GLI3 are a cause of Pallister-Hall syndrome (PHS). Defects in GLI3 are a cause of type A1/B postaxial polydactyly (PAPA1/PAPB). Defects in GLI3 are a cause of type IV preaxial polydactyly. Defects in GLI3 are the cause of acrocallosal syndrome (ACS). The antibody is specific to GLI3. At the molecular level, Gli3 is translated into a 190-kDa transcriptional activator (Gli3-190) that undergoes proteolytic processing into a truncated 83-kDa repressor (Gli3-83) lacking C-terminal activation domains. (PMID: 16705181)
|Product Specific Protocols|
|WB protocol for GLI3-Specific antibody 19949-1-AP||Download protocol|
|IHC protocol for GLI3-Specific antibody 19949-1-AP||Download protocol|
|IF protocol for GLI3-Specific antibody 19949-1-AP||Download protocol|
|IP protocol for GLI3-Specific antibody 19949-1-AP||Download protocol|
|FC protocol for GLI3-Specific antibody 19949-1-AP||Download protocol|
|Click here to view our Standard Protocols|
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