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Huntingtin (phospho Ser421) rabbit pAb - ES5727Huntingtin (phospho Ser421) rabbit pAb Sizes: 50L, 100L Catalogue Numbers: ES5727 50, ES5727 100 Citations, Manuals and MSDS Available upon request. Background: huntingtin (HTT) Homo sapiens Huntingtin is a disease gene linked to Huntington's disease, a neurodegenerative disorder characterized by loss of striatal neurons. This is thought to be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a
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Huntingtin (phospho Ser421) rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES5727-50, ES5727-100

Citations, Manuals and MSDS Available upon request.

Background: huntingtin (HTT) Homo sapiens Huntingtin is a disease gene linked to Huntington's disease, a neurodegenerative disorder characterized by loss of striatal neurons. This is thought to be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product. A fairly broad range of trinucleotide repeats (9-35) has been identified in normal controls, and repeat numbers in excess of 40 have been described as pathological. The huntingtin locus is large, spanning 180 kb and consisting of 67 exons. The huntingtin gene is widely expressed and is required for normal development. It is expressed as 2 alternatively polyadenylated forms displaying different relative abundance in various fetal and adult tissues. The larger transcript is approximately 13.7 kb and is expressed predominantly in adult and fetal brain whereas the smaller transcript of approximately 10.3 kb is more widel

Alternate Name: HTT; HD; IT15; Huntingtin; Huntington disease protein; HD protein

Source: Rabbit

Applications: IHC; IF; ELISA

Dilution: Immunohistochemistry: 1/100 - 1/300. ELISA: 1/5000. Not yet tested in other applications.

Reactivity: Human; Mouse; Rat

Immunogen: The antiserum was produced against synthesized peptide derived from human Huntingtin around the phosphorylation site of Ser421. AA range:387-436

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Human Gene ID: 3064

Human SWISS Prot NO: P42858

Subcellular Location: [Huntingtin]: Cytoplasm. Nucleus. Early endosome. The mutant Huntingtin protein colocalizes with AKAP8L in the nuclear matrix of Huntington disease neurons. Shuttles between cytoplasm and nucleus in a Ran GTPase-independent manner (PubMed:15654337). Recruits onto early endosomes in a Rab5- and HAP40-dependent fashion (PubMed:16476778).; [Huntingtin, myristoylated N-terminal fragment]: Cytoplasmic vesicle, autophagosome.

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Huntingtin (phospho Ser421) rabbit pAb - ES5727

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