CLIP2 anticorps (C-Term)

N° du produit ABIN1537648

Détail du produit anti-CLIP2 anticorps

Antigène: CLIP2 (CAP-GLY Domain Containing Linker Protein 2 (CLIP2))

Épitope: AA 911-940, C-Term

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CLIP2 est non-conjugé

Application: Western Blotting (WB)

Homologie: Rat

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This CYLN2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 911-940 amino acids from the C-terminal region of human CYLN2.

Clone: RB20933

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: CYLN2 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur CLIP2

Antigène: CLIP2 (CAP-GLY Domain Containing Linker Protein 2 (CLIP2))

Autre désignation: CYLN2 (CLIP2 Produits)

Synonymes: anticorps CLIP, anticorps CLIP-115, anticorps CYLN2, anticorps WBSCR3, anticorps WBSCR4, anticorps WSCR3, anticorps WSCR4, anticorps Cyln2, anticorps B230327O20, anticorps Clip1, anticorps mKIAA0291, anticorps wbscr4, anticorps CAP-Gly domain containing linker protein 2, anticorps CAP-GLY domain containing linker protein 2, anticorps CLIP2, anticorps Clip2, anticorps clip2

Sujet: The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.

Poids moléculaire: 115837

ID gène: 7461

NCBI Accession: NP_003379, NP_115797

UniProt: Q9UDT6

Pathways: Dynamique des Microtubules