ASNA1 Rabbit Polyclonal Antibody
cat.: HA500051
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, FC
Clonality: Polyclonal
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.
Storage buffer: 1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: Predicted band size: 39 kDa
Isotype: IgG
Immunogen: Synthetic peptide within human ASNA1 aa 300-348.
Positive control: MCF-7 cell lysate, 293T cell lysate, 293T.
Subcellular location: Cytoplasm, Endoplasmic reticulum, Nucleus.
Recommended Dilutions:
  WB
  IF-Cell
  FC

1:500-1:1,000
1:100
1:1,000
Uniprot #: SwissProt: O43681 Human | G3V9T7 Rat
Alternative names: ARSA 1 ARSA ArsA arsenite transporter ATP binding homolog 1 ArsA arsenite transporter, ATP binding, E. coli, homolog of, 1 ArsA arsenite transporter, ATP-binding, homolog 1 (bacterial) ARSA I ARSA-I ARSA1 ARSAI Arsenical pump driving ATPase Arsenical pump-driving ATPase Arsenical resistance ATPase Arsenite translocating ATPase Arsenite transporting ATPase Arsenite-stimulated ATPase ASNA 1 ASNA I ASNA-I ASNA_HUMAN ASNA1 Asna1 protein ASNAI ATPase ASNA1 GET3 Golgi to ER traffic 3 homolog hARSA-I hASNA-I MGC3821 Transmembrane domain recognition complex 40 kDa ATPase subunit Transmembrane domain recognition complex, 40kDa TRC40
Images
HA500051_1.jpg Fig1: Western blot analysis of ASNA1 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (HA500051, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.
Positive control:
Lane 1: MCF-7 cell lysate
Lane 2: 293T cell lysate
HA500051_2.jpg Fig2: Immunocytochemistry analysis of 293T cells labeling ASNA1 with Rabbit anti-ASNA1 antibody (HA500051) at 1/100 dilution.

Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 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-ASNA1 antibody (HA500051) at 1/100 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 (HA601187, 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.
HA500051_3.jpg Fig3: Flow cytometric analysis of 293T cells labeling ASNA1.

Cells were fixed and permeabilized. Then stained with the primary antibody (HA500051, 1/1,000) (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).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.