SUMF1 antibody (N-Term)

Catalog No. ABIN2789756

Product Details anti-SUMF1 Antibody

Target: SUMF1 (Sulfatase Modifying Factor 1 (SUMF1))

Binding Specificity: N-Term

Reactivity: Human, Mouse, Rat, Cow, Dog, Horse, Guinea Pig, Rabbit

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SUMF1 antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: SREANAPGPV PGERQLAHSK MVPIPAGVFT MGTDDPQIKQ DGEAPARRVT

Predicted Reactivity: Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 93%, Rabbit: 100%, Rat: 100%

Characteristics: This is a rabbit polyclonal antibody against SUMF1. It was validated on Western Blot.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N-terminal region of Human SUMF1

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

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

Handling Advice: Avoid repeat freeze-thaw cycles.

Storage: -20 °C

Storage Comment: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Target Details for SUMF1

Target: SUMF1 (Sulfatase Modifying Factor 1 (SUMF1))

Alternative Name: SUMF1 (SUMF1 Products)

Synonyms: AAPA3037 antibody, FGE antibody, AA543204 antibody, AI463102 antibody, AI851573 antibody, sulfatase modifying factor 1 antibody, SUMF1 antibody, Sumf1 antibody

Background: This gene encodes an enzyme that catalyzes the hydrolysis of sulfate esters by oxidizing a cysteine residue in the substrate sulfatase to an active site 3-oxoalanine residue, which is also known as C-alpha-formylglycine. Mutations in this gene cause multiple sulfatase deficiency, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants.
Alias Symbols: AAPA3037, FGE
Protein Interaction Partner: UBC,
Protein Size: 374

Molecular Weight: 41 kDa

Gene ID: 285362

NCBI Accession: NM_182760, NP_877437

UniProt: Q8NBK3