Stra8 Recombinant Rabbit Monoclonal Antibody [PSH04-55]
Catalog# HA722154
Stra8 Recombinant Rabbit Monoclonal Antibody [PSH04-55]
-
WB
-
IF-Cell
-
FC
-
Human
-
unconjugated
Overview
Product Name
Stra8 Recombinant Rabbit Monoclonal Antibody [PSH04-55]
Antibody Type
Recombinant Rabbit monoclonal Antibody
Immunogen
Recombinant protein within human Stra8 aa 1-330 / 330.
Species Reactivity
Human
Validated Applications
WB, IF-Cell, FC
Target Molecular Weight
Predicted band size: 37 kDa
Positive Control
SK-OV-3 cell lysate, LNCaP cell lysate, SK-OV-3.
Conjugation
unconjugated
Clone Number
PSH04-55
Reactivity Data
| WB | IF-Cell | FC | |
|---|---|---|---|
| Human |
|
|
|
| Mouse |
|
||
| Rat |
|
Product Features
Form
Liquid
Concentration
1 mg/mL.(The concentration of this product may be batch-dependent)
Storage Instructions
Shipped at 4℃. Store at +4℃ short term (1-2 weeks). Store at -20℃ long term.
Storage Buffer
PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Isotype
IgG
Purification Method
Protein A affinity purified.
Application Dilution
-
WB
-
1:1,000
-
IF-Cell
-
1:250
-
FC
-
1:1,000
Target
Function
The signaled by retinoic acid 8 (Stra8) gene is activated only upon stimulation by retinoic acid and expresses a cytoplasmic protein in the gonads of male and female vertebrates. This protein functions to initiate the transition between mitosis and meiosis, aiding in spermatogenesis and oogenesis. In females, its signaling begins 12.5 days after conception, is localized in the primordial germ cells of female ovaries, and ushers in the first stage of meiosis. Male expression begins postnatally and continues throughout life, matching the need of spermatogenesis compared to the limited window of oogenesis in females. Sperm of mice that had induced null mutations for Stra8 gene were able to undergo mitotic divisions, and while some sperm were able to transition into the early stages of meiosis I, but could not transition into further sub-stages of meiosis I. Errors in chromosome pairing and chromosome condensation were observed following these failures. In female mice, loss of Stra8 signaling shows failure to enter into meiosis. Both males and females are left infertile if Stra8 signaling is absent.
Background References
1. Shimada R et al. STRA8-RB interaction is required for timely entry of meiosis in mouse female germ cells. Nat Commun. 2023 Oct
2. Sun S et al. Znhit1 controls meiotic initiation in male germ cells by coordinating with Stra8 to activate meiotic gene expression. Dev Cell. 2022 Apr
Subcellular Location
Cytoplasm, Nucleus.
UNIPROT
Synonyms
Stimulated by retinoic acid 8 antibody
stimulated by retinoic acid 8 homolog antibody
Stimulated by retinoic acid Gene 8 antibody
stimulated by retinoic acid gene 8 homolog antibody
Stimulated by retinoic acid gene 8 protein homolog antibody
STRA 8 antibody
STRA8 antibody
STRA8_HUMAN antibody
Images
-
Western blot analysis of Stra8 on different lysates with Rabbit anti-Stra8 antibody (HA722154) at 1/1,000 dilution.
Lane 1: SK-OV-3 cell lysate
Lane 2: LNCaP cell lysate
Lysates/proteins at 30 µg/Lane.
Predicted band size: 37 kDa
Observed band size: 35 kDa
Exposure time: 3 minutes; ECL: K1802;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA722154) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. -
Immunocytochemistry analysis of SK-OV-3 cells labeling Stra8 with Rabbit anti-Stra8 antibody (HA722154) at 1/250 dilution.
Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Stra8 antibody (HA722154) at 1/250 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.
Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution. -
Flow cytometric analysis of SK-OV-3 cells labeling Stra8.
Cells were fixed and permeabilized. Then stained with the primary antibody (HA722154, 1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"