CLIP2 antibody (C-Term)

Catalog No. ABIN1537648

Product Details anti-CLIP2 Antibody

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

Binding Specificity: AA 911-940, C-Term

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CLIP2 antibody is un-conjugated

Application: Western Blotting (WB)

Predicted Reactivity: Rat

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

Immunogen: 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

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

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

Expiry Date: 6 months

Target Details for CLIP2

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

Alternative Name: CYLN2 (CLIP2 Products)

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

Background: 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.

Molecular Weight: 115837

Gene ID: 7461

NCBI Accession: NP_003379, NP_115797

UniProt: Q9UDT6

Pathways: Microtubule Dynamics