Key Product Details

Species Reactivity

Validated:

Human

Cited:

Human, Mouse, Rat, Transgenic Mouse

Applications

Validated:

Western Blot, Simple Western

Cited:

Immunohistochemistry, Immunohistochemistry-Paraffin, Western Blot, Flow Cytometry, Immunocytochemistry, Immunoprecipitation, IHC-F

Label

Unconjugated

Antibody Source

Polyclonal Goat IgG
Loading...

Product Specifications

Immunogen

E. coli-derived recombinant human PLZF
Met1-Gln254
Accession # Q05516

Specificity

Detects human PLZF in direct ELISAs and Western blots.

Clonality

Polyclonal

Host

Goat

Isotype

IgG

Scientific Data Images for Human PLZF Antibody

Detection of Human PLZF antibody by Western Blot.

Detection of Human PLZF by Western Blot.

Western blot shows lysates of HUVEC human umbilical vein endothelial cells, HEL 92.1.7 human erythroleukemic cell line, LNCaP human prostate cancer cell line, and 293T human embryonic kidney cell line. PVDF membrane was probed with 1 µg/mL of Goat Anti-Human PLZF Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2944) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF019). A specific band was detected for PLZF at approximately 85 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.

Detection of Human PLZF antibody by Simple WesternTM.

Detection of Human PLZF by Simple WesternTM.

Simple Western lane view shows lysates of LNCaP human prostate cancer cell line, loaded at 0.2 mg/mL. A specific band was detected for PLZF at approximately 94 kDa (as indicated) using 10 µg/mL of Goat Anti-Human PLZF Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2944) followed by 1:50 dilution of HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF109). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.

Detection of Mouse PLZF by Western Blot

Detection of Mouse PLZF by Western Blot

Increased mTORC1 activity in germ cells from Lkb1 newborn cKO testis. (a) Western blot of testis proteins at different postnatal ages using specific antibodies against p-S6K1 (T389), p-rpS6 (S235/6), rpS6 and beta -tubulin. rpS6, and beta -tubulin were used as internal controls. (b) Expression of PI3K-, mTOR- and SPC-related markers by western blot in P8 testes from control and Lkb1 cKO mice. (c) Immunohistochemistry for VASA, GATA4, p-rpS6 in P8 control testis. (d) Immunohistochemistry for Lin28a and p-rpS6 in P8 control testis. Serial sections were used in order to compare cellular localizations of these markers in the same tubule. Asterisks, different distribution of Lin28a and p-rpS6 in the same tubule resulting in strong positive for Lin28a and weak staining for p-rpS6. Arrows, cells expressing both Lin28a and p-rpS6. (e) Immunohistochemistry for Plzf and p-rpS6 in control and cKO mice. (f) Mean number of Plzf- or p-rpS6-positive cells in each tubule (positive cells/total tubules). The data were shown as mean±S.E.M. of at least three replicates. *P<0.05. Scale bars=50 μm Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/29022902), licensed under a CC-BY license. Not internally tested by R&D Systems.
Detection of Mouse PLZF by Western Blot

Detection of Mouse PLZF by Immunohistochemistry

Depletion of SPCs in Lkb1 cKO mice. Seminiferous tubules from 5- (a) and 13- (b) week-old control and Lkb1 cKO mice (n=3) were used for immunostaining using specific antibodies against PCNA, gamma H2AX and Plzf. Scale bars=50 μm. Arrows, representative Plzf-positive cells in tubules. (c) Quantification of Plzf-positive germ cells in each tubule. Data are presented as mean±S.E.M. **P < 0. 01 Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/29022902), licensed under a CC-BY license. Not internally tested by R&D Systems.
Detection of PLZF by Western Blot

Detection of PLZF by Western Blot

PGR regulates a network of transcription factors in granulosa cells including Pparg and Zbtb16. (A) Heatmap showing expression level of PGR-regulated transcription factors, including DNA-binding transcription factors (bold) and transcription cofactors (not bold). Shown are PRKO (left) and PRWT (right) RNA-seq reads (LCPM) with blue representing low expression levels and red increased expression levels. (B) Expression of Pparg and Zbtb16 in wildtype granulosa cells over a preovulatory time course from 0–12 h post-hCG using CBA-F1 mice. (C) Expression of Pparg and Zbtb16 in granulosa cells of PRKO (left) PRAKO (center) and PRBKO (right) mice at 8 h post-hCG qPCR data normalized to reference gene Rpl19 and expressed as fold change relative to 0 h or WT control. N = 4 biological replicates of cells pooled from ovaries of 3 females. (D) Western blot for ZBTB16 protein in granulosa cells of PRKO, PRAKO and PRBKO mice at 10 h post-hCG. (E) Quantification of Western blot ZBTB16 expression relative to B-actin loading control. N = 3 pools of cells from 3 females. Mean ± SEM, statistical significance determined by one-way ANOVA. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/35563869), licensed under a CC-BY license. Not internally tested by R&D Systems.
Detection of PLZF by Western Blot

Detection of PLZF by Western Blot

PGR regulates a network of transcription factors in granulosa cells including Pparg and Zbtb16. (A) Heatmap showing expression level of PGR-regulated transcription factors, including DNA-binding transcription factors (bold) and transcription cofactors (not bold). Shown are PRKO (left) and PRWT (right) RNA-seq reads (LCPM) with blue representing low expression levels and red increased expression levels. (B) Expression of Pparg and Zbtb16 in wildtype granulosa cells over a preovulatory time course from 0–12 h post-hCG using CBA-F1 mice. (C) Expression of Pparg and Zbtb16 in granulosa cells of PRKO (left) PRAKO (center) and PRBKO (right) mice at 8 h post-hCG qPCR data normalized to reference gene Rpl19 and expressed as fold change relative to 0 h or WT control. N = 4 biological replicates of cells pooled from ovaries of 3 females. (D) Western blot for ZBTB16 protein in granulosa cells of PRKO, PRAKO and PRBKO mice at 10 h post-hCG. (E) Quantification of Western blot ZBTB16 expression relative to B-actin loading control. N = 3 pools of cells from 3 females. Mean ± SEM, statistical significance determined by one-way ANOVA. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/35563869), licensed under a CC-BY license. Not internally tested by R&D Systems.

Applications for Human PLZF Antibody

Application
Recommended Usage

Simple Western

10 µg/mL
Sample: LNCaP human prostate cancer cell line

Western Blot

1 µg/mL
Sample: HUVEC human umbilical vein endothelial cells, HEL 92.1.7 human erythroleukemic cell line, LNCaP human prostate cancer cell line, and 293T human embryonic kidney cell line

Formulation, Preparation, and Storage

Purification

Antigen Affinity-purified

Reconstitution

Reconstitute at 0.2 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.


Loading...

Formulation

Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.

Shipping

Lyophilized product is shipped at ambient temperature. Liquid small pack size (-SP) is shipped with polar packs. Upon receipt, store immediately at the temperature recommended below.

Stability & Storage

Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 6 months, -20 to -70 °C under sterile conditions after reconstitution.

Calculators

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

=
÷

Background: PLZF

Human PLZF is a 74 kDa nuclear protein that belongs to the POK family of transcriptional repressors. It is a 673 amino acid protein that contains an N-terminal BTB domain, followed by an acidic domain, a proline-rich region and a C-terminal zinc-finger domain. PLZF forms homodimers with RAR alpha and LAZ3 with its zinc-finger region. Alternate splice forms exist which are tissue-specific and show a deletion of either the BTB domain, the acidic region, or the proline-rich region. Human PLZF shares 96%, 97%, 96%, and 96% amino acid identity with rat, mouse, canine, and bovine PLZF, respectively.

Long Name

Promyelocytic Leukemia Zinc Finger

Alternate Names

ZBTB16, ZNF145

Entrez Gene IDs

7704 (Human); 235320 (Mouse)

Gene Symbol

ZBTB16

UniProt

Additional PLZF Products

Product Documents for Human PLZF Antibody

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot or batch number in the search box below.

Note: Certificate of Analysis not available for kit components.

Product Specific Notices for Human PLZF Antibody

For research use only

Citations for Human PLZF Antibody

Customer Reviews for Human PLZF Antibody

There are currently no reviews for this product. Be the first to review Human PLZF Antibody and earn rewards!

Have you used Human PLZF Antibody?

Submit a review and receive an Amazon gift card!

$25/€18/£15/$25CAN/¥2500 Yen for a review with an image

$10/€7/£6/$10CAN/¥1110 Yen for a review without an image

Submit a review
Amazon Gift Card

FAQs

No product specific FAQs exist for this product.

View all FAQs for Antibodies