anti AIBZIP antibody, anti cAMP responsive element binding protein 3-like 4, JAL, hJAL, ATCE1, CREB3, CREB4, androgen-induced basic leucine zipper antibody, anti RP11-422P24.8 antibody, anti OTTHUMP00000035266 antibody, anti cAMP responsive element binding protein 1 antibody
Goat polyclonal antibody to CREB3L4
Klonalität:
Polyclonal
Molekulargewicht:
43.4, 41.3
Puffer:
Supplied at 0.5 mg/ml in Tris saline, 0.02% sodium azide, pH 7.3 with 0.5% bovine serum albumin. Aliquot and store at -20C. Minimize freezing and thawing.
Sequenz:
PSGRIRSVLHADEM
Target-Kategorie:
AIBZIP / CREB3L4
Application Verdünnung:
ELISA: 1:32000, WB: 0.5-2 µg/ml, IHC-P: 2-4µg/ml
Anwendungsbeschreibung:
Application Notes: ELISA: Peptide ELISA: antibody detection limit dilution 1:32000.IHC: In paraffin embedded Human Prostate shows strong staining of cytoplasm in the secretory cells of the gland. Recommended concentration, 2-4ug/ml.WB: Approx 50kDa band observed in Human Placenta lysate (predicted MW of 45kDa according to NP_570968). Recommended for use at 0.5-2 µg/ml
orb18675 (2.5ug/ml) staining of paraffin embedded Human Prostate. Steamed an
2.5 µg/ml staining of paraffin embedded Human Prostate. Steamed antigen retrieval with citrate buffer pH6, AP-staining.
Primary incubation 1 hour at room temperature. Images A, B: MDA-MB-231, A431 cell lysate at primary Ab concentration 0.1 µg/ml, Image C: MCF7 cell lysate at primary Ab concentration 0.003 µg/ml. (Loaded 35 µg protein in RIPA buffer, per lane). Detected by chemiluminescence.
Primary incubation 1 hour at room temperature. Images A, B: Human Kidney and Placenta lysate at primary Ab concentration 0.5 µg/ml. (Loaded 35 µg protein in RIPA buffer, per lane). Detected by chemiluminescence.
Immunofluorescence analysis of paraformaldehyde fixed U2OS cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/ml) followed by Alexa Fluor 488 secondary antibody (2 ug/ml), showing nuclear, nuclear membrane and cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/ml) followed by Alexa Fluor 488 secondary antibody (2 ug/ml).
Immunofluorescence analysis of paraformaldehyde fixed A431 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/ml) followed by Alexa Fluor 488 secondary antibody (2 ug/ml), showing nuclear membrane and cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/ml) followed by Alexa Fluor 488 secondary antibody (2 ug/ml).
Flow cytometric analysis of paraformaldehyde fixed A431 cells (blue line), permeabilized with 0.5% Triton. Primary incubation 1hr (10 ug/ml) followed by Alexa Fluor 488 secondary antibody (1 ug/ml). IgG control: Unimmunized goat IgG (black line) followed by Alexa Fluor 488 secondary antibody.
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