		Technical Data
A1363-01A	ALS2CR1 (Amyotrophic Lateral Sclerosis 2 (juvenile) Chromosome Region, candidate 1, NIF3L1, NIF3 NGG1 interacting factor 3-like 1 (S. pombe), CALS-7, MDS015, NIF3 (Ngg1 interacting factor 3, S.pombe homolog)-like 1)

Description:
Amyotrophic lateral sclerosis chromosomal region candidate gene protein 1 (ALSCR1) or NIF3-like protein1 is a 39kD cytoplasmic protein that participates in neuronal differentiation. The ALS2CR1 full-lengh transcrip is encoded within the ALS2 critical region, however, experimental evidences indicate that ALS2CR1 is not causative gene for amyotrophic lateral sclerosis (ALS20).

Applications:
Suitable for use in ELISA and Western Blot. Other applications not tested.

Recommended Dilution:
ELISA: 1:32000
Western Blot: 0.2-1ug/ml
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.

Type	Isotype	Clone	Grade
Pab			Affinity Purified

Size		Storage	Shipping	Source	Host
100ug		-20°C	Blue Ice	Human	Goat

Concentration:

As reported

Immunogen:

Synthetic peptide corresponding to ALS2CR1.

Purity:

Purified by immunoaffinity chromatography.

Form

Supplied as a liquid in Tris-saline, pH 7.2, 0.5% BSA, 0.02% sodium azide.

Specificity:

Recognizes human ALS2CR1 at ~40kD in Human Heart and Human Testis extracts (predicted MW of approx. 39kD according to NP_068596). Species Crossreactivity: Mouse.

Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.

1. Hadano S, Yanagisawa Y, Skaug J, Fichter K, Nasir J, Martindale D, Koop BF, Scherer SW, Nicholson DW, Rouleau GA, Ikeda J, Hayden MR. Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2. Genomics. 2001 Jan 15;71(2):200-13.