NF-H Recombinant Antibody [JF99-07] - Rat IgG1 (Chimeric) - BSA and Azide free
cat.: HA610394
Product Type: Recombinant Chimeric Antibody, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P, IF-Tissue
Clone number: JF99-07
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*PBS (pH7.4).
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 112 kDa
Immunogen: Synthetic peptide within human NEFH aa 690-740.
Positive control: Mouse cerebellum tissue lysate, Rat brain tissue lysate, mouse cerebellum tissue, rat cerebellum tissue.
Subcellular location: Cytoplasm, cytoskeleton, Cell projection, axon.
Recommended Dilutions:
  WB
  IHC-P
  IF-Tissue

1:2,000
1:500-1:2,000
1:500
Uniprot #: SwissProt: P12036 Human | P19246 Mouse | P16884 Rat
Alternative names: 200 kDa neurofilament protein CMT2CC Nefh Neurofilament heavy polypeptide 200kDa Neurofilament heavy polypeptide Neurofilament triplet H protein NF H NF-H NFH NFH_HUMAN
Images
HA610394_1.jpg Fig1: Western blot analysis of NF-H on different lysates with Rat anti-NF-H antibody (HA610394) at 1/2,000 dilution.

Lane 1: Mouse cerebellum tissue lysate (10 µg/Lane)
Lane 2: Rat brain tissue lysate (20 µg/Lane)

Predicted band size: 112 kDa
Observed band size: 200 kDa

Exposure time: 5 seconds; ECL: K1801;

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 (HA610394) at 1/2,000 dilution was used in primary antibody dilution (K1803) at 4℃ overnight. Goat Anti-Rat IgG H&L - HRP Secondary Antibody (HA1023) at 1/50,000 dilution was used for 1 hour at room temperature.
HA610394_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded mouse cerebellum tissue with Rat anti-NF-H antibody (HA610394) at 1/2,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA610394) at 1/2,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
HA610394_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded rat cerebellum tissue with Rat anti-NF-H antibody (HA610394) at 1/2,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA610394) at 1/2,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
HA610394_4.jpg Fig4: Application: IF-Tissue

Species: Human

Site: brain

Sample: Paraffin-embedded section

Antibody concentration: 1/500
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.