ALMS1 rabbit pAb
This gene encodes a protein containing a large tandem-repeat domain as well as additional low complexity regions. The encoded protein functions in microtubule organization, particularly in the formation and maintanance of cilia. Mutations in this gene cause Alstrom syndrome. There is a pseudogene for this gene located adjacent in the same region of chromosome 2. Alternative splice variants have been described but their full length nature has not been determined. [provided by RefSeq, Apr 2014],
Product Specifications
Background
UniProt
Q8TCU4
Swiss Prot
Q8TCU4
Reactivity
Human; Rat; Mouse
Immunogen
Synthesized peptide derived from ALMS1 . at AA range: 1530-1610
Clonality
Polyclonal
Source
Rabbit
Applications
WB; IHC; IF; ELISA
Concentration
1 mg/ml
Dilution
Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.
Molecular Weight
460kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
460kD
Fragment
IgG
Subcellular Location
Other Product Names
ALMS1; KIAA0328; Alstrom syndrome protein 1
Gene ID (Human)
7840
Available Sizes
Frequently Asked Questions
Explore Other Products
Browse additional items from our catalog
NOXA, NT (Phorbol-12-myristate-13-acetate-induced Protein 1, PMA-induced Protein 1, Immediate-early-response Protein APR, Protein Noxa, PMAIP1) (HRP) discontinued
Tissue cDNA, First Strand, Human Adult Normal, Brain, Pons, BioGenomicsTM
