Anti-Amyotrophic lateral sclerosis protein 2 (ALS2)

Anti-Amyotrophic lateral sclerosis protein 2 (ALS2)
Item number Size Datasheet Manual SDS Delivery time Quantity Price
A1362-86.1 1 mg - -

3 - 19 business days*

808.00€
 
\Amyotrophic lateral sclerosis protein 2 (ALS2) or Alsin is a 184kD protein that contains three... more
Product information "Anti-Amyotrophic lateral sclerosis protein 2 (ALS2)"
\Amyotrophic lateral sclerosis protein 2 (ALS2) or Alsin is a 184kD protein that contains three guanine-nucleotide exchange factor domains and may act as a GTPase regulator. ALS2 dysfunction affects endosome trafficking through a Rab5 small GTPases family-mediated mechanism. It is a causative gene for a juvenile autosomal recessive form of motor neuron diseases, including amyotrophic lateral sclerosis 2. This disorder is characterized by a progressive degeneration of the upper motor neurons of the motor cortex and the lower motor neurons of the brain stem and spinal cord. Applications: Suitable for use in ELISA. Other applications not tested. Recommended Dilution: ELISA: 1:50, Optimal dilutions to be determined by the researcher. Storage and Stability: May be stored at 4°C for short-term only. For long-term storage and to avoid repeated freezing and thawing, aliquot and store at -20°C. Aliquots are stable for at least 12 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.
Supplier: United States Biological
Supplier-Nr: A1362-86

Properties

Application: ELISA
Antibody Type: Polyclonal
Conjugate: No
Host: Rabbit
Reactivity: Human
Immunogen: Synthetic peptide (LKACYYQIQREKLN) corresponding to aa1644-1657 of human ALS2
Format: Affinity Purified

Database Information

Handling & Safety

Storage: -20°C
Shipping: +4°C (International: +4°C)
Caution
Our products are for laboratory research use only: Not for administration to humans!
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