WHSC1 antibody (AA 525-575)

Catalog No. ABIN7453147

Product Details anti-WHSC1 Antibody

Target: WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))

Binding Specificity: AA 525-575

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This WHSC1 antibody is un-conjugated

Application: Western Blotting (WB)

Purpose: Rabbit anti-NSD2 Antibody, Affinity Purified

Purification: Affinity Purified

Immunogen: between AA 525 and 575

Isotype: IgG

Application Details

Application Notes:

IP: Not recommended

WB: 1:2,000 - 1:10,000

Restrictions: For Research Use only

Handling

Concentration: 200 μg/mL

Buffer: Tris-buffered Saline containing 0.1 % BSA and 0.09 % 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

Expiry Date: 12 months

Target Details for WHSC1

Target: WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))

Alternative Name: NSD2 (WHSC1 Products)

Synonyms: WHSC1 antibody, fc12c04 antibody, wu:fc12c04 antibody, wu:fi20c01 antibody, si:rp71-77d7.2 antibody, whs antibody, nsd2 antibody, trx5 antibody, mmset antibody, reiibp antibody, MMSET antibody, NSD2 antibody, REIIBP antibody, TRX5 antibody, WHS antibody, RGD1565590 antibody, 5830445G22Rik antibody, 9430010A17Rik antibody, AW555663 antibody, C130020C13Rik antibody, D030027O06Rik antibody, D930023B08Rik antibody, Whsc1l antibody, mKIAA1090 antibody, nuclear receptor binding SET domain protein 2 antibody, Wolf-Hirschhorn syndrome candidate 1 antibody, NSD2 antibody, nsd2 antibody, WHSC1 antibody, Nsd2 antibody

Background: Background: MMSET (multiple myeloma SET domain-containing protein) or NSD2 (nuclear SET-domain containing protein 2) is the product of the Wolf-Hirschhorn syndrome candidate 1 (WHSC1) gene. MMSET is a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development and is a probable histone methyltransferase. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4 [taken from NCBI Entrez Gene (Gene ID: 7468].

Gene ID: 7468

NCBI Accession: NP_579877

UniProt: O96028

Pathways: SARS-CoV-2 Protein Interactome