Septin 9 antibody

Catalog No. ABIN7231314

This anti-Septin 9 antibody is a Rabbit Polyclonal antibody detecting Septin 9 in WB and ELISA. Suitable for Human.

Quick Overview for Septin 9 antibody (ABIN7231314)

Target: Septin 9 (SEPT9)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Septin 9 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-Septin 9 Antibody

Purpose: SEPT9 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of SEPT9 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogen: Synthesized peptide derived from part region of human SEPT9 protein

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: -20 °C

Storage Comment: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Target Details for Septin 9

Target: Septin 9 (SEPT9)

Alternative Name: SEPT9

Background: Rabbit Anti-SEPT9 Polyclonal Antibody,Septin-9, MLL septin-like fusion protein MSF-A, MLL septin-like fusion protein, Ovarian/Breast septin, Ov/Br septin, Septin D1,SEPT9 gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.,SEPT9

Molecular Weight: observerd band 64kDa

Gene ID: 10801

UniProt: Q9UHD8