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Anti-VAPB Antibody (1M998) is a Rabbit antibody targeting VAPB. Anti-VAPB Antibody (1M998) can be used in IHC-P.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 100 μL | $269 | 7-10 days | 7-10 days |
| Description | Anti-VAPB Antibody (1M998) is a Rabbit antibody targeting VAPB. Anti-VAPB Antibody (1M998) can be used in IHC-P. |
| Synonyms | VAP-B, VAMP-B, VAMP (vesicle-associated membrane protein)-associated protein B and C, ALS8 |
| Ig Type | Rabbit IgG |
| Clone | 1M998 |
| Reactivity | Human |
| Specificity | Human VAPB |
| Verified Activity | 1. Immunochemical staining of human VAPB in human pancreas with rabbit monoclonal antibody (1:300, formalin-fixed paraffin embedded sections). 2. Immunochemical staining of human VAPB in human liver with rabbit monoclonal antibody (1:300, formalin-fixed paraffin embedded sections). 3. Immunochemical staining of human VAPB in human cirrhosis with rabbit monoclonal antibody (1:300, formalin-fixed paraffin embedded sections). 4. Immunochemical staining of human VAPB in human brain with rabbit monoclonal antibody (1:300, formalin-fixed paraffin embedded sections). |
| Application | |
| Recommended Dose | IHC-P: 1:100-1:500 |
| Antibody Type | Monoclonal |
| Host Species | Rabbit |
| Construction | This antibody was obtained from a rabbit immunized with purified, recombinant Human VAPB / VAP-B (rh VAPB / VAP-B; TMPY-02196; O95292-1; Met1-Pro132). |
| Purification | Protein A |
| Appearance | Liquid |
| Formulation | 0.2 μm filtered solution in PBS |
| Research Background | Vesicle-associated membrane protein-associated protein B / C, also known as VAMP-B/VAMP-C, VAMP-associated protein B/C, VAP-B/VAP-C and VAPB, is a single-pass type IV membrane protein that belongs to the VAMP-associated protein (VAP) family. VAPB contains one MSP domain. VAPB may play a role in vesicle trafficking. VAPB forms a heterodimer with VAPA. VAPB interacts with VAMP1 and VAMP2. Defects in VAPB are the cause of amyotrophic lateral sclerosis type 8 ( ALS8 ) which is a familial form of amyotrophic lateral sclerosis, a neurodegenerative disorder affecting upper and lower motor neurons and resulting in fatal paralysis. Defects in VAPB are also a cause of spinal muscular atrophy autosomal dominant Finkel type (SMAF) which is characterized by proximal muscle weakness that begins in the lower limbs and then progresses to upper limbs. |
| Conjucates | Unconjugated |
| Immunogen | Recombinant Protein: Human VAPB/VAP-B Protein (TMPY-02196) |
| Antigen Species | Human |
| Stability & Storage | Store at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. Preservative-Free. |
| Transport | Shipping with blue ice. |
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