Cytochrome b5 (CYTB5) (AA 9-80) antibody (Biotin)

Catalog No. ABIN709903

Product Details

Target: Cytochrome b5 (CYTB5)

Binding Specificity: AA 9-80

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Dog,Cow,Sheep,Pig

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human Cytochrome b5

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

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

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details

Target: Cytochrome b5 (CYTB5)

Alternative Name: Cytochrome b5 (CYTB5 Products)

Synonyms: CYB5 antibody, MCB5 antibody, Cyb5 antibody, 0610009N12Rik antibody, Cyb5a antibody, CYB5A antibody, 1857 antibody, BcDNA:GH02503 antibody, BcDNA:RE66521 antibody, CG2140 antibody, CYT-B5 antibody, CYTB5 antibody, Dmel\\CG2140 antibody, dpld antibody, l(2)01857 antibody, l(2)k00107 antibody, cytochrome b5 type A antibody, cytochrome b5 type A (microsomal) antibody, cytochrome b5 antibody, Cytochrome b5 antibody, CYB5A antibody, Cyb5a antibody, LOC100328915 antibody, LOC100735904 antibody, Cyt-b5 antibody

Background:

Synonyms: CYB 5, CYB 5A, CYB5, CYB5_HUMAN, CYB5A, Cytochrome b 5, Cytochrome b5 microsomal, Cytochrome b5, Cytochrome b5 type A microsomal, Cytochrome b5 type A, MCB 5, MCB5, Microsomal cytochrome b5, Microsomal cytochrome b5 type A, Type 1 cyt b5, CYB5A.

Background: The protein encoded by this gene is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl-CoA-desaturase activity. Defects in this gene are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]

Gene ID: 1528