Septin 9 antibody (AA 1-110)

Catalog No. ABIN6147560

Product Details anti-Septin 9 Antibody

Target: Septin 9 (SEPT9)

Binding Specificity: AA 1-110

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Septin 9 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Sequence: MEPPASKVPE VPTAPATDAA PKRVEIQMPK PAEAPTAPSP AQTLENSEPA PVSQLQSRLE PKPQPPVAEA TPRSQEATEA APSCVGDMAD TPRDAGLKQA PASRNEKAPV

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-110 of human Septin 9 (NP_001106964.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IF,1:50 - 1:200

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for Septin 9

Target: Septin 9 (SEPT9)

Alternative Name: 9-Sep (SEPT9 Products)

Synonyms: SEPT9 antibody, msf antibody, msf1 antibody, napb antibody, sint1 antibody, pnutl4 antibody, septd1 antibody, af17q25 antibody, septin-9 antibody, AF17q25 antibody, MSF antibody, MSF1 antibody, NAPB antibody, PNUTL4 antibody, SINT1 antibody, SeptD1 antibody, Msf antibody, Sint1 antibody, Eseptin antibody, Slpa antibody, cb999 antibody, fb02h06 antibody, sept9 antibody, wu:fb02h06 antibody, septin 9 antibody, septin-9 antibody, septin 9 S homeolog antibody, septin 9a antibody, SEPT9 antibody, sept9 antibody, LOC100605286 antibody, sept9.S antibody, Sept9 antibody, sept9a antibody

Background: This 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,AF17q25,MSF,MSF1,NAPB,PNUTL4,SINT1,SeptD1,septin-9,Cell Biology & Developmental Biology,Cell Cycle,Immunology & Inflammation,Cytokines,9-Sep

Molecular Weight: 38 kDa/41 kDa/47 kDa/52 kDa/63 kDa/64 kDa/65 kDa

Gene ID: 10801

UniProt: Q9UHD8