ALMS1 Polyclonal antibody

ALMS1 Polyclonal Antibody for FC, IF, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

IF, FC, ELISA

Conjugate

Unconjugated

Cat no : 27231-1-AP

Synonyms

ALMS1, ALSS, Alstrom syndrome 1, Alstrom syndrome protein 1, KIAA0328

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Validation Data Gallery

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  IF Staining of HeLa using 27231-1-AP

  Immunofluorescent analysis of (-20°C Ethanol) fixed HeLa cells using 27231-1-AP (ALMS1 antibody) at dilution of 1:50 and Alexa Fluor 488-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L).

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  FC experiment of HeLa using 27231-1-AP

  1X10^6 HeLa cells were stained with 0.20ug ALMS1 antibody (27231-1-AP, red) and control antibody (blue). Fixed with 90% MeOH.

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Tested Applications

• Positive IF detected in: HeLa cells
• Positive FC detected in: HeLa cells

Recommended dilution

• Immunofluorescence (IF): IF : 1:50-1:500

Sample-dependent, check data in validation data gallery

Product Information

27231-1-AP targets ALMS1 in IF, FC, ELISA applications and shows reactivity with human samples.

• Tested Reactivity: human
• Host / Isotype: Rabbit / IgG
• Class: Polyclonal
• Type: Antibody
• Immunogen: ALMS1 fusion protein Ag26100
• Full Name: Alstrom syndrome 1
• Calculated molecular weight: 461 kDa
• GenBank accession number: NM_015120
• Gene symbol: ALMS1
• Gene ID (NCBI): 7840
• Conjugate: Unconjugated
• Form: Liquid
• Purification Method: Antigen affinity purification
• Storage Buffer: PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
• Storage Conditions: Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20^oC storage. 20ul sizes contain 0.1% BSA.

Background Information

ALMS1 (Alstrom syndrome protein 1) is also KIAA0328. ALMS1 encodes a ~ 0.5 megadalton protein that localises to the base of centrioles. Some studies have suggested a role for this protein in maintaining centriole-nucleated sensory organelles termed primary cilia, and AS is now considered to belong to the growing class of human genetic disorders linked to ciliary dysfunction (ciliopathies). The ALMS1 protein is a component of the centrosome (PMID:30421101). ALMS1 is involved in PCM1-dependent intracellular transport. ALMS1 is required, directly or indirectly, for the localization of NCAPD2 to the proximal ends of centrioles. It is required for proper formation and/or maintenance of primary cilia (PC), microtubule-based structures that protrude from the surface of epithelial cells.